CN1227229C - Ethylene derivatives and pest controlling agents - Google Patents

Ethylene derivatives and pest controlling agents Download PDF

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Publication number
CN1227229C
CN1227229C CNB97194041XA CN97194041A CN1227229C CN 1227229 C CN1227229 C CN 1227229C CN B97194041X A CNB97194041X A CN B97194041XA CN 97194041 A CN97194041 A CN 97194041A CN 1227229 C CN1227229 C CN 1227229C
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alkyl
arbitrarily
replaced
phenyl
group
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CN1216530A (en
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小仓友幸
村上博
沼田昭
宫地理香
三宅敏郎
三森纪彦
泷井新自
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Nissan Chemical Corp
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    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
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    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
    • A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
    • A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
    • A01N43/10—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings with sulfur as the ring hetero atom
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    • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
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    • A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
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    • A01N47/06—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom containing —O—CO—O— groups; Thio analogues thereof
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    • A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
    • A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
    • A01N47/12—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, neither directly attached to a ring nor the nitrogen atom being a member of a heterocyclic ring
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    • A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
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    • A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
    • A01N57/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
    • A01N57/16—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing heterocyclic radicals
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    • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
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    • C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • C07D277/22—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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Abstract

Ethylene derivatives of formula (I) where Q is an unsubstituted or substituted phenyl or heterocyclic group, especially a 4-thiazolyl, 1- or 3-pyrazolyl, 1,3-oxazol-4-yl, phenyl or pyridyl group; E is a substituent such as a cyano group; A is a substituent such as a 4-pyrazolyl or thiazolyl group; and B is a substituent such as an alkylcarbonyl group. Agricultural chemicals and agents for preventing the attachment of aquatic organisms containing one or more such ethylene derivatives.

Description

Ethene derivatives and the pesticides that contains this derivative
Technical field
The present invention relates to new ethene derivatives, and contain to adhere to and prevent agent as the agricultural chemicals of this compound of activeconstituents and hydrobiont.Agricultural chemicals is meant and comprises insecticide, miticide, nematocides, weedicide and mycocide etc. herein, particularly is applied to the pesticides in agricultural, gardening, livestock industry and the health field.Hydrobiont adheres to and prevents that agent from being the chemical that is used to prevent that harmful hydrobiont (as shell and marine alga) from adhering to, and the described position of adhering to generation is cooling water inlet passage, underwater structure and the reservoir of heat exchanger of circulating water system, the chemical industry of fishing net, hull bottom, Offshore Units (as buoy), ship structure, heat and atomic energy apparatus.
Background technology
With regard to acrylonitrile derivative, disclose 2 among the clear 53-92769 of Japanese Patent Application Laid-Open '-chloro-3-hydroxyl-2-(4-phenyl-2-thiazolyl)-cinnamyl nitrile is as the purposes of sterilant; And the purposes of this compound as the hydrobiont adhesion inhibitors disclosed among the open WO95/29591 of international patent application.The purposes of 2-(4-chloro-phenyl-)-3-(3-pyridyl)-3-oxypropionitrile as sterilant disclosed among the clear 60-11452 of Japanese Patent Application Laid-Open; And the purposes of this compound as mycocide disclosed among the clear 60-11401 of Japanese Patent Application Laid-Open.
With regard to the life-time service of sterilant and mycocide, recently, some harmful organisms become chemical are had tolerance, and are difficult to usually eliminate with conventional sterilant and mycocide; In addition, some toxicity of pesticide is big, and is easy to extended residual under Undec situation, thereby the ecosystem is produced destruction; Therefore, all expect sterilant and the mycocide short that development makes new advances, low toxicity for a long time with long-lasting.
On the other hand, in order to prevent the hydrobiological adhesion and the growth of seawater and fresh water, use the antifouling paint that contains organo-tin compound (as two (tributyl tin) oxide compound) or copper compound (as copper sulfate or Red copper oxide); But although can effectively prevent hydrobiological adhesion, the toxicity of organo-tin compound is big, and especially is easy in fish and shellfish body inner accumulated, owing to aggravated environmental pollution, controls the use of this compound at present with law; Copper compound is widely used in the antifouling paint of access road and hull bottom; But, similar to tin compound, contain copper in the copper compound as heavy metal; Therefore, the use of copper compound will cause following environmental pollution, and contain this class copper compound and adhere to as hydrobiont and prevent that agent from being can not be preferred.In sum, need influentially to the ecosystem hardly, and cause the hydrobiont of secondary pollution to adhere to hardly preventing agent.
Disclosure of an invention
In order to address the above problem, the inventor is diligent to be devoted to agricultural chemicals and hydrobiont are adhered to the research that prevents agent, described chemical and prevent that agent from just can demonstrate desinsection (bacterium) activity of excellence when a small amount of the use, and nontarget organism (as Mammals, fish and useful worm) is not almost had negative impact; As a result, find that compound hereinafter described has high security, has excellent desinsection (bacterium) activity and prevents the activity that hydrobiont adheres to.Based on above-mentioned discovery, the inventor has finished the present invention.
Specifically, the invention provides following [1] to [25]:
[1] formula (I) ethene derivatives:
Figure C9719404100141
[wherein:
The phenyl that the Q representative is replaced by G arbitrarily, (described heterocyclic radical is a thienyl to the naphthyl that is replaced by G, or the heterocyclic radical that is replaced by R arbitrarily arbitrarily, furyl, pyrryl oxazolyl isoxazolyl, thiazolyl, isothiazolyl, pyrazolyl, imidazolyl, 1,3,4-oxadiazole base, 1,2,4-oxadiazole base, 1,3, the 4-thiadiazolyl group, 1,2, the 4-thiadiazolyl group, 1,2, the 4-triazolyl, 1,2, the 3-thiadiazolyl group, 1,2, the 3-triazolyl, 1,2,3, the 4-tetrazyl, pyridyl, pyrimidyl, pyrazinyl, pyridazinyl, 1,3, the 5-triazinyl, 1,2, the 4-triazinyl, 1,2,4,5-tetrazine base, pyrazolinyl, imidazolinyl oxazolinyl isoxazoline-3-yl, thiazolinyl, imidazolone, imidazolidimedione, 3 (2H)-pyridazinones, benzothiazolyl, benzimidazolyl-, indazolyl benzoxazolyl, quinolyl, isoquinolyl, quinoxalinyl, 2, the 3-phthalazinyl, cinnoline base or quinazolyl);
The phenyl that the A representative is replaced by W arbitrarily, (described heterocyclic radical is a thienyl to the naphthyl that is replaced by W, or the heterocyclic radical that is replaced by Y arbitrarily arbitrarily, furyl, pyrryl oxazolyl isoxazolyl, thiazolyl, isothiazolyl, pyrazolyl, imidazolyl, 1,3,4-oxadiazole base, 1,2,4-oxadiazole base, 1,3, the 4-thiadiazolyl group, 1,2, the 4-thiadiazolyl group, 1,2, the 4-triazolyl, 1,2, the 3-thiadiazolyl group, 1,2, the 3-triazolyl, 1,2,3, the 4-tetrazyl, pyridyl, pyrimidyl, pyrazinyl, pyridazinyl, 1,3, the 5-triazinyl, 1,2, the 4-triazinyl, 1,2,4,5-tetrazine base, pyrazolinyl, imidazolinyl oxazolinyl isoxazoline-3-yl, thiazolinyl, 3 (2H)-pyridazinones, benzothiazolyl, benzimidazolyl-, indazolyl benzoxazolyl, quinolyl, isoquinolyl, quinoxalinyl, 2, the 3-phthalazinyl, cinnoline base or quinazolyl);
Condition is: (a) when Q be the thienyl that is replaced by R arbitrarily, the furyl that is replaced by R arbitrarily, arbitrarily when quinolyl that is replaced by R or the isoquinolyl that replaced by R arbitrarily, A is the phenyl that is replaced by W arbitrarily, (described heterocyclic radical is a pyrryl oxazolyl isoxazolyl to the naphthyl that is replaced by W, or the heterocyclic radical that is replaced by Y arbitrarily arbitrarily, thiazolyl, isothiazolyl, pyrazolyl, imidazolyl, 1,3,4-oxadiazole base, 1,2,4-oxadiazole base, 1,3, the 4-thiadiazolyl group, 1,2, the 4-thiadiazolyl group, 1,2, the 4-triazolyl, 1,2, the 3-thiadiazolyl group, 1,2, the 3-triazolyl, 1,2,3, the 4-tetrazyl, pyrimidyl, pyrazinyl, pyridazinyl, 1,3, the 5-triazinyl, 1,2, the 4-triazinyl, pyrazolinyl, imidazolinyl oxazolinyl isoxazoline-3-yl, thiazolinyl, 3 (2H)-pyridazinones, benzothiazolyl, benzimidazolyl-, indazolyl benzoxazolyl, quinoxalinyl, 2, the 3-phthalazinyl, cinnoline base or quinazolyl);
(b) when Q is the 2-thiazolyl that is replaced by R arbitrarily, A is that (described heterocyclic radical is a thienyl for the naphthyl that is replaced by W arbitrarily or the heterocyclic radical that is replaced by Y arbitrarily, furyl, pyrryl oxazolyl isoxazolyl, thiazolyl, isothiazolyl, pyrazolyl, imidazolyl, 1,3,4-oxadiazole base, 1,2,4-oxadiazole base, 1,3, the 4-thiadiazolyl group, 1,2, the 4-thiadiazolyl group, 1,2, the 4-triazolyl, 1,2, the 3-thiadiazolyl group, 1,2, the 3-triazolyl, 1,2,3, the 4-tetrazyl, pyridyl, pyrimidyl, pyrazinyl, pyridazinyl, 1,3, the 5-triazinyl, 1,2, the 4-triazinyl, pyrazolinyl, imidazolinyl oxazolinyl isoxazoline-3-yl, thiazolinyl, 3 (2H)-pyridazinones, benzothiazolyl, benzimidazolyl-, indazolyl benzoxazolyl, quinolyl, isoquinolyl, quinoxalinyl, 2, the 3-phthalazinyl, cinnoline base or quinazolyl);
(c) when Q was the pyridyl that is replaced by R arbitrarily, A was that (described heterocyclic radical is a pyrryl oxazolyl isoxazolyl to the heterocyclic radical that is replaced by Y arbitrarily, thiazolyl, isothiazolyl, pyrazolyl, imidazolyl, 1,3,4-oxadiazole base, 1,2,4-oxadiazole base, 1,3, the 4-thiadiazolyl group, 1,2, the 4-thiadiazolyl group, 1,2, the 4-triazolyl, 1,2, the 3-thiadiazolyl group, 1,2, the 3-triazolyl, 1,2,3, the 4-tetrazyl, pyrazinyl, 1,3, the 5-triazinyl, 1,2, the 4-triazinyl, pyrazolinyl, imidazolinyl oxazolinyl isoxazoline-3-yl, thiazolinyl, 3 (2H)-pyridazinones, benzothiazolyl, benzimidazolyl-, indazolyl benzoxazolyl, quinoxalinyl, 2, the 3-phthalazinyl, cinnoline base or quinazolyl);
(d) when Q be the isothiazolyl that is replaced by R arbitrarily, arbitrarily by R replace 1,2, when 3-triazolyl or the benzoxazolyl that replaced by R arbitrarily, A is that (described heterocyclic radical is a thienyl for the naphthyl that is replaced by W arbitrarily or the heterocyclic radical that is replaced by Y arbitrarily, furyl, pyrryl oxazolyl isoxazolyl, thiazolyl, isothiazolyl, pyrazolyl, imidazolyl, 1,3,4-oxadiazole base, 1,2,4-oxadiazole base, 1,3, the 4-thiadiazolyl group, 1,2, the 4-thiadiazolyl group, 1,2, the 4-triazolyl, 1,2, the 3-thiadiazolyl group, 1,2, the 3-triazolyl, 1,2,3, the 4-tetrazyl, pyridyl, pyrimidyl, pyrazinyl, pyridazinyl, 1,3, the 5-triazinyl, 1,2, the 4-triazinyl, pyrazolinyl, imidazolinyl oxazolinyl isoxazoline-3-yl, thiazolinyl, 3 (2H)-pyridazinones, benzothiazolyl, benzimidazolyl-, indazolyl benzoxazolyl, quinolyl, isoquinolyl, quinoxalinyl, 2, the 3-phthalazinyl, cinnoline base or quinazolyl);
(e) when Q be arbitrarily by R replace 1,2, during the 4-triazolyl, A is that (described heterocyclic radical is a thienyl to the heterocyclic radical that is replaced by Y arbitrarily, furyl, pyrryl oxazolyl isoxazolyl, thiazolyl, isothiazolyl, pyrazolyl, imidazolyl, 1,3,4-oxadiazole base, 1,2,4-oxadiazole base, 1,3, the 4-thiadiazolyl group, 1,2, the 4-thiadiazolyl group, 1,2, the 4-triazolyl, 1,2, the 3-thiadiazolyl group, 1,2, the 3-triazolyl, 1,2,3, the 4-tetrazyl, pyrimidyl, pyrazinyl, pyridazinyl, 1,3, the 5-triazinyl, 1,2, the 4-triazinyl, pyrazolinyl, imidazolinyl oxazolinyl isoxazoline-3-yl, thiazolinyl, 3 (2H)-pyridazinones, benzothiazolyl, benzimidazolyl-, indazolyl benzoxazolyl, quinolyl, isoquinolyl, quinoxalinyl, 2, the 3-phthalazinyl, cinnoline base or quinazolyl);
(f) when Q is the benzothiazolyl that is replaced by R arbitrarily, A is that (described heterocyclic radical is a furyl for the naphthyl that is replaced by W arbitrarily or the heterocyclic radical that is replaced by Y arbitrarily, pyrryl oxazolyl isoxazolyl, thiazolyl, isothiazolyl, pyrazolyl, imidazolyl, 1,3,4-oxadiazole base, 1,2,4-oxadiazole base, 1,3, the 4-thiadiazolyl group, 1,2, the 4-thiadiazolyl group, 1,2, the 4-triazolyl, 1,2, the 3-thiadiazolyl group, 1,2, the 3-triazolyl, 1,2,3, the 4-tetrazyl, pyridyl, pyrimidyl, pyrazinyl, pyridazinyl, 1,3, the 5-triazinyl, 1,2, the 4-triazinyl, pyrazolinyl, imidazolinyl oxazolinyl isoxazoline-3-yl, thiazolinyl, 3 (2H)-pyridazinones, benzothiazolyl, benzimidazolyl-, indazolyl benzoxazolyl, quinolyl, isoquinolyl, quinoxalinyl, 2, the 3-phthalazinyl, cinnoline base or quinazolyl);
(g) when Q is the benzimidazolyl-that is replaced by R arbitrarily, A is that (described heterocyclic radical is a pyrryl oxazolyl isoxazolyl for the naphthyl that is replaced by W arbitrarily or the heterocyclic radical that is replaced by Y arbitrarily, thiazolyl, isothiazolyl, pyrazolyl, imidazolyl, 1,3,4-oxadiazole base, 1,2,4-oxadiazole base, 1,3, the 4-thiadiazolyl group, 1,2, the 4-thiadiazolyl group, 1,2, the 4-triazolyl, 1,2, the 3-thiadiazolyl group, 1,2, the 3-triazolyl, 1,2,3, the 4-tetrazyl, pyrazinyl, 1,3, the 5-triazinyl, 1,2, the 4-triazinyl, pyrazolinyl, imidazolinyl oxazolinyl isoxazoline-3-yl, thiazolinyl, 3 (2H)-pyridazinones, benzothiazolyl, benzimidazolyl-, indazolyl benzoxazolyl, quinolyl, isoquinolyl, quinoxalinyl, 2, the 3-phthalazinyl, cinnoline base or quinazolyl);
(h) when Q was the phenyl that is replaced by G arbitrarily, A was that (described heterocyclic radical is a pyrryl oxazolyl isoxazolyl to the heterocyclic radical that is replaced by Y arbitrarily, thiazolyl, isothiazolyl, pyrazolyl, 1,3,4-oxadiazole base, 1,2,4-oxadiazole base, 1,3, the 4-thiadiazolyl group, 1,2, the 4-thiadiazolyl group, 1,2, the 4-triazolyl, 1,2, the 3-thiadiazolyl group, 1,2, the 3-triazolyl, 1,2,3, the 4-tetrazyl, pyrazinyl, pyridazinyl, 1,3, the 5-triazinyl, 1,2, the 4-triazinyl, pyrazolinyl, imidazolinyl oxazolinyl isoxazoline-3-yl, thiazolinyl, 3 (2H)-pyridazinones, benzothiazolyl, benzimidazolyl-, indazolyl benzoxazolyl, quinoxalinyl, 2, the 3-phthalazinyl, cinnoline base or quinazolyl);
(i) when Q was the naphthyl that is replaced by G arbitrarily, A was that (described heterocyclic radical is a thienyl to the heterocyclic radical that is replaced by Y arbitrarily, pyrryl oxazolyl isoxazolyl, thiazolyl, isothiazolyl, pyrazolyl, imidazolyl, 1,3,4-oxadiazole base, 1,2,4-oxadiazole base, 1,3, the 4-thiadiazolyl group, 1,2, the 4-thiadiazolyl group, 1,2, the 4-triazolyl, 1,2, the 3-thiadiazolyl group, 1,2, the 3-triazolyl, 1,2,3, the 4-tetrazyl, pyridyl, pyrimidyl, pyrazinyl, pyridazinyl, 1,3, the 5-triazinyl, 1,2, the 4-triazinyl, pyrazolinyl, imidazolinyl oxazolinyl isoxazoline-3-yl, thiazolinyl, 3 (2H)-pyridazinones, benzothiazolyl, benzimidazolyl-, indazolyl benzoxazolyl, quinolyl, isoquinolyl, quinoxalinyl, 2, the 3-phthalazinyl, cinnoline base or quinazolyl);
B represents H, C 1-C 4Alkyl, C 1-C 4Haloalkyl, C 2-C 4Alkoxyalkyl, CH 3SCH 2, CH 3OC 2H 4OCH 2, the C that is replaced by phenyl 1-C 4Alkyl, and described phenyl is arbitrarily by halogen or C 1-C 4Alkyl replaces, the C that is replaced by benzoyl 1-C 4Alkyl, and described benzoyl is arbitrarily by halogen or C 1-C 4Alkyl replaces, THP trtrahydropyranyl, (CH 3) 3Si, C 1-C 4Alkyl sulphonyl is arbitrarily by halogen or C 1-C 4The benzenesulfonyl that alkyl replaces ,-SO 2CF 3, C 1-C 4The alkyl monosubstituted amino alkylsulfonyl, C 2-C 8Dialkyl amino sulfonyl, phenyl amino alkylsulfonyl, C 2-C 5The alkyl monosubstituted amino thiocarbonyl, C 3-C 9The dialkyl amido thiocarbonyl, C 2-C 5The cyano group alkyl, C 3-C 9Alkoxy carbonyl alkyl ,-C (=O) T 1,-P (=O) T 2T 3,-P (=S) T 2T 3, alkali metal atom, alkaline earth metal atom, or NHT 4T 5T 6
Condition is: when Q was 2-thiazolyl or 2-[4-morpholinodithio base, B was C 1-C 4Alkyl, C 1-C 4Haloalkyl, C 2-C 4Alkoxyalkyl, CH 3SCH 2, CH 3OC 2H 4OCH 2, the C that is replaced by phenyl 1-C 4Alkyl, and described phenyl is arbitrarily by halogen or C 1-C 4Alkyl replaces, the C that is replaced by benzoyl 1-C 4Alkyl, and described benzoyl is arbitrarily by halogen or C 1-C 4Alkyl replaces, THP trtrahydropyranyl, (CH 3) 3Si, C 1-C 4Alkyl sulphonyl is arbitrarily by halogen or C 1-C 4The benzenesulfonyl that alkyl replaces ,-SO 2CF 3, C 1-C 4The alkyl monosubstituted amino alkylsulfonyl, C 2-C 8Dialkyl amino sulfonyl, phenyl amino alkylsulfonyl, C 2-C 5The alkyl monosubstituted amino thiocarbonyl, C 3-C 9The dialkyl amido thiocarbonyl, C 2-C 5The cyano group alkyl, C 3-C 9Alkoxy carbonyl alkyl ,-C (=O) T 1,-P (=O) T 2T 3, or-P (=S) T 2T 3
The E representative is arbitrarily by C 1-C 4Alkyl or C 1-C 4(described heterocyclic radical is 2-oxazolyl, 2-thiazolyl, 2-imidazolyl, 1,2 to the heterocyclic radical that haloalkyl replaces, 4-triazole-3-base, 1,2,4-oxadiazole-3-base, 1,2,4-thiadiazoles-3-base, 1,3,4-oxadiazole-2-base, 5-tetrazyl, 2-oxazolinyl or 1,2,4, or represent halogen, C 5-tetrazine-3-yl), 2-C 4Alkynyl, the phenylacetylene base that is replaced by Z arbitrarily, C 1-C 4Haloalkyl, CN, isonitrile base, NO 2, N 3, CHO, C 2-C 5Alkyl-carbonyl, C 2-C 5Carbalkoxy, C 3-C 5The alkenyloxy carbonyl, C 2-C 4Alkyl amino-carbonyl, C 3-C 9Dialkyl amino carbonyl, the benzoyl that is replaced by Z arbitrarily, amino thiocarbonyl, C 1-C 4Alkylthio, C 1-C 4Alkyl sulphinyl, C 1-C 4Alkyl sulphonyl, the thiophenyl that is replaced by Z arbitrarily, the benzenesulfinyl that is replaced by Z arbitrarily, the benzenesulfonyl that is replaced by Z arbitrarily ,-P (=O) T 2T 3, or-P (=S) T 2T 3The benzenesulfinyl that is replaced by Z arbitrarily, the benzenesulfonyl that is replaced by Z arbitrarily ,-P (=O) T 2T 3, or-P (=S) T 2T 3
G is the substituting group that freely is selected from following radicals: halogen atom, C 1-C 10Alkyl, C 2-C 4The cyano group alkyl, the C that is replaced by phenyl 1-C 4Alkyl, and described phenyl is arbitrarily by halogen or C 1-C 4Alkyl replaces, C 2-C 6Alkenyl, C 2-C 6Alkynyl, C 1-C 6Haloalkyl, C 2-C 6Halogenated alkenyl, C 2-C 6The halo alkynyl, C 3-C 6Halogenated cycloalkyl is arbitrarily by C 1-C 3The C that alkyl replaces 3-C 6Cycloalkyl, C 1-C 10Alkoxyl group, C 2-C 6Alkenyloxy, C 2-C 6Alkynyloxy group, C 1-C 4Halogenated alkoxy, C 2-C 6The halo alkenyloxy, C 2-C 6The halo alkynyloxy group, C 1-C 4Alkylthio, C 1-C 4Alkyl sulphinyl, C 1-C 4Alkyl sulphonyl, C 2-C 6Alkenyl thio, C 2-C 6The alkenyl sulfinyl, C 2-C 6The alkenyl alkylsulfonyl, C 2-C 6The alkynes sulfenyl, C 2-C 6The alkynyl sulfinyl, C 2-C 6The alkynyl alkylsulfonyl, C 1-C 4Halogenated alkylthio, C 1-C 4The haloalkyl sulfinyl, C 1-C 4Halogenated alkyl sulfonyl, C 2-C 6The halo alkenyl thio, C 2-C 6The halogenated alkenyl sulfinyl, C 2-C 6The halogenated alkenyl alkylsulfonyl, C 2-C 6The acetylenic halide sulfenyl, C 2-C 6Halo alkynyl sulfinyl, C 2-C 6Halo alkynyl alkylsulfonyl, CHO, NO 2, CN ,-NU 1U 2, OH, naphthyl, the methoxyl group that is replaced by phenyl, and described phenyl is arbitrarily by halogen or C 1-C 4Alkyl replaces, C 2-C 7Carbalkoxy, C 2-C 4Alkoxyalkyl, C 2-C 4Alkyl-carbonyl, C 2-C 4Halogenated alkyl carbonyl, C 2-C 5Alkyl carbonyl oxy, C 2-C 5Haloalkyl carbonyl oxygen base, C 3-C 7Dialkyl amido carbonyl oxygen base; the phenyl that is replaced by Z arbitrarily; the phenoxy group that is replaced by Z arbitrarily; the benzoyl that is replaced by Z, the pyridyl that is replaced by Z, the pyridyloxy that is replaced by Z arbitrarily arbitrarily arbitrarily; the thienyl that is replaced by Z arbitrarily; be bonded in the methylene-dioxy on adjacent the position of substitution, be bonded on adjacent the position of substitution the halo methylene-dioxy and-N=CT 7T 8(T wherein 7And T 8Independent separately H or phenyl, benzyl or the C of representing 1-C 6Alkyl, or T 7And T 8Carbon atom with institute's bonding forms 5,6,7 or 8 yuan of rings), (condition is when substituting group is two or more, and described substituting group can be identical or different), and the quantity of substituting group G is 1,2,3 or 4; Or G is bonded in the alkylidene group that forms 5,6,7 or 8 yuan of rings on adjacent the position of substitution;
R is the substituting group that freely is selected from following radicals: halogen atom, C 1-C 10Alkyl, the C that is replaced by phenyl 1-C 4Alkyl, and described phenyl is arbitrarily by halogen or C 1-C 4Alkyl replaces, C 2-C 6Alkenyl, C 2-C 6Alkynyl, C 1-C 6Haloalkyl, C 2-C 6Halogenated alkenyl, C 2-C 6The halo alkynyl, C 3-C 6Halogenated cycloalkyl is arbitrarily by C 1-C 3The C that alkyl replaces 3-C 6Cycloalkyl, C 1-C 6Alkoxyl group, C 2-C 6Alkenyloxy, C 2-C 6Alkynyloxy group, C 1-C 4Halogenated alkoxy, C 2-C 6The halo alkenyloxy, C 2-C 6The halo alkynyloxy group, C 1-C 4Alkylthio, C 1-C 4Alkyl sulphinyl, C 1-C 4Alkyl sulphonyl, C 2-C 6Alkenyl thio, C 2-C 6The alkenyl sulfinyl, C 2-C 6The alkenyl alkylsulfonyl, C 2-C 6The alkynes sulfenyl, C 2-C 6The alkynyl sulfinyl, C 2-C 6The alkynyl alkylsulfonyl, C 1-C 4Halogenated alkylthio, C 1-C 4The haloalkyl sulfinyl, C 1-C 4Halogenated alkyl sulfonyl, C 2-C 6The halo alkenyl thio, C 2-C 6The halogenated alkenyl sulfinyl, C 2-C 6The halogenated alkenyl alkylsulfonyl, C 2-C 6The acetylenic halide sulfenyl, C 2-C 6Halo alkynyl sulfinyl, C 2-C 6Halo alkynyl alkylsulfonyl, NO 2, CN ,-NU 1U 2, phenoxy group, OH, naphthyl, C 2-C 7Carbalkoxy, C 2-C 4Alkoxyalkyl, C 2-C 4Alkyl-carbonyl, C 2-C 5Alkyl carbonyl oxy, C 2-C 5Haloalkyl carbonyl oxygen base, the benzoyl that is replaced by X arbitrarily, the phenyl that is replaced by X arbitrarily, the pyridyl that is replaced by X arbitrarily, arbitrarily the thienyl that is replaced by X and-N=CT 7T 8(condition is when substituting group is two or more, and described substituting group can be identical or different), and the quantity of substituent R is 1,2,3 or 4; Or R is bonded on adjacent the position of substitution to form the alkylidene group of 5,6,7 or 8 yuan of rings;
Y is the substituting group that freely is selected from following radicals: halogen atom, C 1-C 10Alkyl, C 1-C 6Haloalkyl, C 1-C 6Alkoxyl group, C 2-C 6Alkenyloxy, C 2-C 6Alkynyloxy group, C 1-C 4Halogenated alkoxy, C 2-C 6The halo alkenyloxy, C 2-C 6The halo alkynyloxy group, C 1-C 4Alkylthio, C 1-C 4Alkyl sulphinyl, C 1-C 4Alkyl sulphonyl, C 2-C 6Alkenyl thio, C 2-C 6The alkenyl sulfinyl, C 2-C 6The alkenyl alkylsulfonyl, C 2-C 6The alkynes sulfenyl, C 2-C 6The alkynyl sulfinyl, C 2-C 6The alkynyl alkylsulfonyl, C 1-C 4Halogenated alkylthio, C 1-C 4The haloalkyl sulfinyl, C 1-C 4Halogenated alkyl sulfonyl, C 2-C 6The halo alkenyl thio, C 2-C 6The halogenated alkenyl sulfinyl, C 2-C 6The halogenated alkenyl alkylsulfonyl, C 2-C 6The acetylenic halide sulfenyl, C 2-C 6Halo alkynyl sulfinyl, C 2-C 6Halo alkynyl alkylsulfonyl, NO 2, CN ,-NU 1U 2, OH, C 2-C 7Carbalkoxy, C 2-C 4Alkoxyalkyl, C 2-C 5Alkyl carbonyl oxy, C 2-C 5Haloalkyl carbonyl oxygen base, C 3-C 7Dialkyl amido carbonyl oxygen base, arbitrarily the phenyl that is replaced by X and-N=CT 7T 8(T wherein 7And T 8Independent separately H or phenyl, benzyl or the C of representing 1-C 6Alkyl, or T 7And T 8Can form 5,6,7 or 8 yuan of rings with the carbon atom of institute's bonding), (condition is when substituting group is two or more, and described substituting group can be identical or different), and the quantity of substituting group Y is 1,2,3 or 4; Or Y is bonded on adjacent the position of substitution to form the alkylidene group of 5,6,7 or 8 yuan of rings;
W is the substituting group that freely is selected from following radicals: halogen atom, C 1-C 6Alkyl, C 1-C 4Haloalkyl, C 1-C 4Alkoxyl group, C 1-C 4Halogenated alkoxy, C 1-C 4Alkylthio, C 1-C 4Alkyl sulphinyl, C 1-C 4Alkyl sulphonyl, C 1-C 4Halogenated alkylthio, C 1-C 4The haloalkyl sulfinyl, C 1-C 4Halogenated alkyl sulfonyl, C 2-C 4Alkenyl, C 2-C 4Halogenated alkenyl, C 2-C 4Alkenyloxy, C 2-C 4The halo alkenyloxy, C 2-C 4Alkenyl thio, C 2-C 4The alkenyl sulfinyl, C 2-C 4The alkenyl alkylsulfonyl, C 2-C 4The halo alkenyl thio, C 2-C 4The halogenated alkenyl sulfinyl, C 2-C 6The halogenated alkenyl alkylsulfonyl, C 2-C 4Alkynyl, C 2-C 4The halo alkynyl, C 2-C 4Alkynyloxy group, C 2-C 4The halo alkynyloxy group, C 2-C 4The alkynes sulfenyl, C 2-C 4The alkynyl sulfinyl, C 2-C 4The alkynyl alkylsulfonyl, C 2-C 4The acetylenic halide sulfenyl, C 2-C 4Halo alkynyl sulfinyl, C 2-C 4Halo alkynyl alkylsulfonyl, NO 2, CN, formyl radical, C 2-C 6Carbalkoxy, C 2-C 6Alkyl-carbonyl, C 2-C 6Halogenated alkyl carbonyl, C 2-C 6Alkyl oxy carbonyl oxygen and-NU 1U 2, (condition is when substituting group is two or more, and described substituting group can be identical or different), and the quantity of substituting group W is 1,2,3 or 4;
T 1Represent C 1-C 20Alkyl, C 2-C 6Alkenyl, C 1-C 6Haloalkyl, C 1-C 4Alkoxy-C 1-C 4Alkyl, C 3-C 6Halogenated cycloalkyl, the C that is replaced by phenyl 1-C 4Alkyl, and described phenyl is arbitrarily by halogen or C 1-C 4Alkyl replaces, arbitrarily by C 1-C 3The C that alkyl replaces 3-C 6Cycloalkyl, the cycloalkyl that is replaced by phenyl, and described phenyl is arbitrarily by halogen or C 1-C 4Alkyl replaces, by phenyl and C 1-C 4The common cyclopropyl that replaces of alkyl, and described phenyl is arbitrarily by halogen or C 1-C 4Alkyl replaces, by phenyl and the common C that replaces of halogen 3-C 4Cycloalkyl, and described phenyl is arbitrarily by halogen or C 1-C 4Alkoxyl group replaces, by C 2-C 4Alkenyl and C 1-C 4The common cyclopropyl that replaces of alkyl, and described C 2-C 4Alkenyl is replaced by halogen arbitrarily, the C that is replaced by phenyl 2-C 4Alkenyl, and described phenyl is arbitrarily by halogen or C 1-C 4Alkyl replaces, C 1-C 12Alkoxyl group, C 1-C 4Halogenated alkoxy, C 2-C 5Alkenyloxy is arbitrarily by C 1-C 3The C that alkyl replaces 3-C 6Cycloalkyloxy, benzyloxy, C 2-C 5Carbalkoxy ,-NU 1U 2, phenyl amino, the phenyl that is replaced by Z arbitrarily, the phenoxy group that is replaced by Z, the thiophenyl that is replaced by Z, the naphthyl that is replaced by Z arbitrarily arbitrarily arbitrarily, or 5 yuan of being replaced by Z arbitrarily or 6 yuan of heterocyclic radicals (described heterocyclic radical is selected from thienyl, furyl, pyrryl oxazolyl isoxazolyl, thiazolyl, isothiazolyl, pyrazolyl, imidazolyl, 1,3,4-oxadiazole base, 1,2,4-oxadiazole base, 1,3, the 4-thiadiazolyl group, 1,2, the 4-thiadiazolyl group, 1,2, the 4-triazolyl, 1,2, the 3-thiadiazolyl group, 1,2, the 3-triazolyl, 1,2,3, the 4-tetrazyl, pyridyl, pyrimidyl, pyrazinyl, pyridazinyl, 1,3, the 5-triazinyl, 1,2, the 4-triazinyl, pyrazolinyl, imidazolinyl oxazolinyl isoxazoline-3-yl, thiazolinyl and 3 (2H)-pyridazinone);
T 2And T 3Independently represent OH, phenyl, C separately 1-C 6Alkyl, C 1-C 6Alkoxyl group or C 1-C 4Alkylthio;
T 4, T 5And T 6The independent separately H, C of representing 1-C 6Alkyl, C 2-C 6Alkenyl is arbitrarily by C 1-C 3The C that alkyl replaces 3-C 6Cycloalkyl, or benzyl; Or T 4, T 5And T 6In any two can form 5,6,7 or 8 yuan of cyclic groups with the nitrogen-atoms of institute's bonding, and described cyclic group contains aerobic, nitrogen and/or sulphur atom arbitrarily;
X and Z freely are selected from halogen atom, C independently 1-C 4Alkyl, C 1-C 4Haloalkyl, C 1-C 4Alkoxyl group, C 1-C 4Halogenated alkoxy, C 1-C 4Alkylthio, C 1-C 4Alkyl sulphinyl, C 1-C 4Alkyl sulphonyl, C 2-C 5Alkenyl thio, C 2-C 5The alkenyl sulfinyl, C 2-C 5The alkenyl alkylsulfonyl, C 1-C 4Halogenated alkylthio, C 1-C 4The haloalkyl sulfinyl, C 1-C 4Halogenated alkyl sulfonyl, NO 2, CN, CHO, OH ,-NU 1U 2, phenyl, phenoxy group, C 2-C 5Carbalkoxy, (condition is when substituting group is two or more, and described substituting group can be identical or different), and the quantity of substituent X and Z each naturally 1,2,3,4 or 5;
T 7And T 8Independently represent H separately, or phenyl, benzyl, or C 1-C 6Alkyl; Or T 7And T 8Can form 5,6,7 or 8 yuan of rings with the carbon atom of institute's bonding; And
U 1And U 2The independent separately H, C of representing 1-C 6Alkyl, C 2-C 5Alkyl-carbonyl, phenyl or benzyl; Or U 1And U 2Can form 5,6,7 or 8 yuan of rings with the nitrogen-atoms of institute's bonding.
[2] ethene derivatives of above-mentioned [1], wherein:
Q is the phenyl that is replaced by G arbitrarily, the naphthyl that is replaced by G, or the heterocyclic radical that is replaced by R arbitrarily arbitrarily, described heterocyclic radical is a thienyl, furyl, pyrryl oxazolyl isoxazolyl, thiazolyl, isothiazolyl, pyrazolyl, imidazolyl, 1,3,4-oxadiazole base, 1,2,4-oxadiazole base, 1,3, the 4-thiadiazolyl group, 1,2, the 4-thiadiazolyl group, 1,2, the 4-triazolyl, 1,2, the 3-triazolyl, 1,2,3, the 4-tetrazyl, pyridyl, pyrimidyl, pyrazinyl, pyridazinyl, 1,3, the 5-triazinyl, 1,2, the 4-triazinyl, 1,2,4,5-tetrazine base, pyrazolinyl, imidazolinyl, imidazolone or imidazolidimedione base;
A is the phenyl that is replaced by W arbitrarily, the naphthyl that is replaced by W, or the heterocyclic radical that is replaced by Y arbitrarily arbitrarily, described heterocyclic radical is a thienyl, furyl, pyrryl oxazolyl isoxazolyl, thiazolyl, isothiazolyl, pyrazolyl, imidazolyl, 1,3,4-oxadiazole base, 1,2,4-oxadiazole base, 1,3, the 4-thiadiazolyl group, 1,2, the 4-thiadiazolyl group, 1,2, the 4-triazolyl, 1,2, the 3-thiadiazolyl group, 1,2, the 3-triazolyl, 1,2,3, the 4-tetrazyl, pyridyl, pyrimidyl, pyrazinyl, pyridazinyl, the 1,3,5-triazines base, 1,2, the 4-triazinyl, pyrazolinyl or imidazolinyl;
B is H, C 1-C 4Alkyl, C 1-C 4Haloalkyl, C 2-C 4Alkoxyalkyl, CH 3OC 2H 4OCH 2, C 1-C 4Alkyl sulphonyl is arbitrarily by halogen or C 1-C 4The benzenesulfonyl that alkyl replaces ,-SO 2CF 3, C 2-C 8Dialkyl amino sulfonyl, C 2-C 9The dialkyl amido thiocarbonyl, C 3-C 9Alkoxy carbonyl alkyl ,-C (=O) T 1,-P (=O) T 2T 3,-P (=S) T 2T 3, alkali metal atom, alkaline earth metal atom, or NHT 4T 5T 6
T 1Be C 1-C 20Alkyl, C 2-C 6Alkenyl, C 1-C 4Haloalkyl, C 1-C 4Alkoxy-C 1-C 4Alkyl, the C that is replaced by phenyl 1-C 4Alkyl, and described phenyl is arbitrarily by halogen or C 1-C 4Alkyl replaces, C 3-C 6Halogenated cycloalkyl is arbitrarily by C 1-C 3The C that alkyl replaces 3-C 6Cycloalkyl, the cycloalkyl that is replaced by phenyl, and described phenyl is arbitrarily by halogen or C 1-C 4Alkyl replaces, by phenyl and C 1-C 4The common cyclopropyl that replaces of alkyl, and described phenyl is arbitrarily by halogen or C 1-C 4Alkyl replaces, by the C of phenyl and halogen replacement 3-C 4Cycloalkyl, and described phenyl is arbitrarily by halogen or C 1-C 4Alkoxyl group replaces, by C 2-C 4Alkenyl and C 1-C 4The cyclopropyl that alkyl replaces, and described C 2-C 4Alkenyl is replaced by halogen arbitrarily, the C that is replaced by phenyl 2-C 4Alkenyl, and described phenyl is arbitrarily by halogen or C 1-C 4Alkyl replaces, C 1-C 12Alkoxyl group, C 1-C 4Halogenated alkoxy, C 2-C 5Alkenyloxy is arbitrarily by C 1-C 3The C that alkyl replaces 3-C 6Cycloalkyloxy, benzyloxy, C 2-C 5Carbalkoxy, the phenyl that is replaced by Z arbitrarily, the phenoxy group that is replaced by Z arbitrarily, thiophenyl, naphthyl, or the heterocyclic radical that is replaced by Z arbitrarily, described heterocyclic radical are selected from thienyl, furyl, oxazolyl, thiazolyl, pyrazolyl and pyridyl.
[3] ethene derivatives of above-mentioned [2], wherein
Q is the phenyl that is replaced by G arbitrarily, the naphthyl that is replaced by G, or the heterocyclic radical that is replaced by R arbitrarily arbitrarily, and described heterocyclic radical is
A is the phenyl that is replaced by W arbitrarily, the naphthyl that is replaced by W, or the heterocyclic radical that is replaced by Y arbitrarily arbitrarily, and described heterocyclic radical is
Figure C9719404100261
Figure C9719404100281
Or
Condition is: (a) when Q be Q-1, Q-2, Q-3 or Q-4 any one the time, A is the phenyl that is replaced by W arbitrarily, the naphthyl that is replaced by W, or the heterocyclic radical that is replaced by Y arbitrarily arbitrarily, (described heterocyclic radical is any one of following group:
A-5, A-6, A-7, A-8, A-9, A-10, A-11, A-12, A-13, A-14, A-15, A-16, A-17, A-18, A-19, A-20, A-21, A-22, A-23, A-24, A-25, A-26, A-27, A-28, A-29, A-30, A-31, A-32, A-33, A-34, A-35, A-36, A-37, A-38, A-39, A-40, A-41, A-42, A-43, A-44, A-45, A-46, A-47, A-48, A-49, A-50, A-51, A-52, A-53, A-57, A-58, A-59, A-60, A-61, A-62, A-63, A-64, A-65, A-66, A-67, A-68, A-69, A-70, A-71, A-72, A-73, A-74 or A-75)
(b) when Q is Q-12, A is the naphthyl that is replaced by W arbitrarily, or the heterocyclic radical that is replaced by Y arbitrarily, (described heterocyclic radical is any one of following group:
A-1, A-2, A-3, A-4, A-5, A-6, A-7, A-8, A-9, A-10, A-11, A-12, A-13, A-14, A-15, A-16, A-17, A-18, A-19, A-20, A-21, A-22, A-23, A-24, A-25, A-26, A-27, A-28, A-29, A-30, A-31, A-32, A-33, A-34, A-35, A-36, A-37, A-38, A-39, A-40, A-41, A-42, A-43, A-44, A-45, A-46, A-47, A-48, A-49, A-50, A-51, A-52, A-53, A-54, A-55, A-56, A-57, A-58, A-59, A-60, A-61, A-62, A-63, A-64, A-65, A-66, A-67, A-68, A-69, A-70, A-71, A-72, A-73, A-74 or A-75)
(c) when Q be Q-52, Q-53 or Q-54 any one the time, A is the heterocyclic radical that is replaced by Y arbitrarily, (described heterocyclic radical is any one of following group:
A-5, A-6, A-7, A-8, A-9, A-10, A-11, A-12, A-13, A-14, A-15, A-16, A-17, A-18, A-19, A-20, A-21, A-22, A-23, A-24, A-25, A-26, A-27, A-28, A-29, A-30, A-31, A-32, A-33, A-34, A-35, A-36, A-37, A-38, A-39, A-40, A-41, A-42, A-43, A-44, A-45, A-46, A-47, A-48, A-49, A-50, A-51, A-52, A-53, A-60, A-63, A-64, A-65, A-66, A-67, A-68, A-69, A-70, A-71, A-72, A-73, A-74 or A-75)
(d) when Q be Q-23, Q-24, Q-43, Q-44, Q-45, Q-46 or Q-49 any one the time, A is the naphthyl that is replaced by W arbitrarily, or the heterocyclic radical that is replaced by Y arbitrarily, (described heterocyclic radical is any one of following group: A-1, A-2, A-3, A-4, A-5, A-6, A-7, A-8, A-9, A-10, A-11, A-12, A-13, A-14, A-15, A-16, A-17, A-18, A-19, A-20, A-21, A-22, A-23, A-24, A-25, A-26, A-27, A-28, A-29, A-30, A-31, A-32, A-33, A-34, A-35, A-36, A-37, A-38, A-39, A-40, A-41, A-42, A-43, A-44, A-45, A-46, A-47, A-48, A-49, A-50, A-51, A-52, A-53, A-54, A-55, A-56, A-57, A-58, A-59, A-60, A-61, A-62, A-63, A-64, A-65, A-66, A-67, A-68, A-69, A-70, A-71, A-72, A-73, A-74 or A-75)
(e) when Q be Q-37, Q-38, Q-39, Q-40, Q-41 or Q-42 any one the time, A is the heterocyclic radical that is replaced by Y arbitrarily, (described heterocyclic radical is any one of following group:
A-1, A-2, A-3, A-4, A-5, A-6, A-7, A-8, A-9, A-10, A-11, A-12, A-13, A-14, A-15, A-16, A-17, A-18, A-19, A-20, A-21, A-22, A-23, A-24, A-25, A-26, A-27, A-28, A-29, A-30, A-31, A-32, A-33, A-34, A-35, A-36, A-37, A-38, A-39, A-40, A-41, A-42, A-43, A-44, A-45, A-46, A-47, A-48, A-49, A-50, A-51, A-52, A-53, A-57, A-58, A-59, A-60, A-61, A-62, A-63, A-64, A-65, A-66, A-67, A-68, A-69, A-70, A-71, A-72, A-73, A-74 or A-75)
(f) when Q was the phenyl that is replaced by G arbitrarily, A was the heterocyclic radical that is replaced by Y arbitrarily, and described heterocyclic radical is any one of following group: A-5, A-6, A-7, A-8, A-9, A-10, A-11, A-12, A-13, A-14, A-19, A-20, A-21, A-22, A-23, A-24, A-25, A-26, A-27, A-28, A-29, A-30, A-31, A-32, A-33, A-34, A-35, A-36, A-37, A-38, A-39, A-40, A-41, A-42, A-43, A-44, A-45, A-46, A-47, A-48, A-49, A-50, A-51, A-52, A-53, A-60, A-61, A-62, A-63, A-64, A-65, A-66, A-67, A-68, A-69, A-70, A-71, A-72, A-73, A-74 or A-75
(g) when Q was the naphthyl that is replaced by G arbitrarily, A was the heterocyclic radical that is replaced by Y arbitrarily, and described heterocyclic radical is any one of following group: A-1, A-2, A-5, A-6, A-7, A-8, A-9, A-10, A-11, A-12, A-13, A-14, A-15, A-16, A-17, A-18, A-19, A-20, A-21, A-22, A-23, A-24, A-25, A-26, A-27, A-28, A-29, A-30, A-31, A-32, A-33, A-34, A-35, A-36, A-37, A-38, A-39, A-40, A-41, A-42, A-43, A-44, A-45, A-46, A-47, A-48, A-49, A-50, A-51, A-52, A-53, A-54, A-55, A-56, A-57, A-58, A-59, A-60, A-61, A-62, A-63, A-64, A-65, A-66, A-67, A-68, A-69, A-70, A-71, A-72, A-73, A-74 or A-75
R 1Be selected from: halogen atom, C 1-C 10Alkyl, C 2-C 6Alkenyl, C 2-C 6Alkynyl, C 1-C 6Haloalkyl, C 1-C 6Alkoxyl group, C 2-C 6Alkenyloxy, NO 2, CN ,-NU 1U 2, OH, C 2-C 7Carbalkoxy, C 2-C 4Alkoxyalkyl, C 2-C 4Alkyl-carbonyl, the phenyl that is replaced by X arbitrarily, the pyridyl that is replaced by X arbitrarily, arbitrarily the thienyl that is replaced by X and-N=CT 7T 8(T wherein 7And T 8Independent separately H, phenyl, benzyl or the C of representing 1-C 6Alkyl, or T 7And T 8Can form 5,6,7 or 8 yuan of rings with the carbon atom of institute's bonding), or can form 5,6,7 or 8 yuan of rings as alkylidene group with adjacent substituent R;
Y 1Be selected from: halogen atom, C 1-C 10Alkyl, C 1-C 6Haloalkyl, C 1-C 6Alkoxyl group, C 2-C 6Alkenyloxy, NO 2, CN ,-NU 1U 2, OH, C 2-C 7Carbalkoxy, C 2-C 4Alkoxyalkyl, arbitrarily the phenyl that is replaced by X and-N=CT 7T 8(T wherein 7And T 8Independent separately H or phenyl, benzyl or the C of representing 1-C 6Alkyl, or T 7And T 8Can form 5,6,7 or 8 yuan of rings with the carbon atom of institute's bonding), (condition is when substituting group is two or more, and described substituting group can be identical or different), or can with adjacent Y 1Form 5,6,7 or 8 yuan of rings as alkylidene group together;
X is that quantity is 1 to 4 and freely is selected from the substituting group of following group: halogen atom, C 1-C 4Alkyl, C 1-C 4Haloalkyl, C 1-C 4Alkoxyl group, C 1-C 4Halogenated alkoxy, C 1-C 4Alkylthio, C 1-C 4Alkyl sulphinyl, C 1-C 4Alkyl sulphonyl, C 2-C 5Alkenyl thio, C 2-C 5The alkenyl sulfinyl, C 2-C 5The alkenyl alkylsulfonyl, C 1-C 4Halogenated alkylthio, C 1-C 4The haloalkyl sulfinyl, C 1-C 4Halogenated alkyl sulfonyl, NO 2, CN, CHO, OH ,-NU 1U 2, phenyl, phenoxy group, and C 2-C 5Carbalkoxy, (condition is when the quantity of substituent X is two or more, and described substituting group can be identical or different);
Z is that quantity is 1 to 4 and freely is selected from the substituting group of following group: halogen atom, C 1-C 4Alkyl, C 1-C 4Haloalkyl, C 1-C 4Alkoxyl group, C 1-C 4Halogenated alkoxy, C 1-C 4Alkylthio, C 1-C 4Alkyl sulphinyl, C 1-C 4Alkyl sulphonyl, C 1-C 4Alkenyl thio, C 1-C 4The alkenyl sulfinyl, C 1-C 4The alkenyl alkylsulfonyl, NO 2, CN ,-NU 1U 2, phenyl, phenoxy group, and C 2-C 5Carbalkoxy, (condition is when the quantity of substituting group Z is two or more, and described substituting group can be identical or different);
M represents substituent quantity, and is 0,1,2 or 3;
N represents substituent quantity, and is 0,1,2,3 or 4;
P represents substituent quantity, and is 0,1 or 2;
Q represents substituent quantity, and is 0 or 1;
(condition be when m, n and p each naturally integer 2 or when bigger, described substituting group can be identical or different).
[4] ethene derivatives of above-mentioned [2], wherein E is CN.
[5] ethene derivatives of above-mentioned [3], wherein E is CN.
[6] ethene derivatives of above-mentioned [2], wherein E is arbitrarily by C 1-C 4Alkyl or C 1-C 4The heterocyclic radical that haloalkyl replaces (described heterocyclic radical is 2-oxazolyl, 2-thiazolyl, 2-imidazolyl, 1,2,4-triazole-3-base, 1,2,4-oxadiazole-3-base, 1,2,4-thiadiazoles-3-base or 1,3,4-oxadiazole-2-yl), or halogen atom, C 2-C 4Alkynyl, the phenylacetylene base that is replaced by Z arbitrarily, C 1-C 4Haloalkyl, CN, NO 2, N 3, CHO, C 2-C 5Alkyl-carbonyl, C 2-C 5Carbalkoxy, C 2-C 4Alkyl amino-carbonyl, C 3-C 9Dialkyl amino carbonyl, the benzoyl that is replaced by Z arbitrarily, amino thiocarbonyl, C 1-C 4Alkylthio, C 1-C 4Alkyl sulphinyl, C 1-C 4Alkyl sulphonyl, the thiophenyl that is replaced by Z arbitrarily, the phenyl sulfinyl that is replaced by Z arbitrarily, the benzenesulfonyl that is replaced by Z arbitrarily ,-P (=O) T 2T 3, or-P (=S) T 2T 3
[7] ethene derivatives of above-mentioned [3], wherein E is arbitrarily by C 1-C 4Alkyl or C 1-C 4The heterocyclic radical that haloalkyl replaces (described heterocyclic radical is 2-oxazolyl, 2-thiazolyl, 2-imidazolyl, 1,2,4-triazole-3-base, 1,2,4-oxadiazole-3-base, 1,2,4-thiadiazoles-3-base or 1,3,4-oxadiazole-2-yl), or halogen atom, C 2-C 4Alkynyl, the phenylacetylene base that is replaced by Z arbitrarily, C 1-C 4Haloalkyl, CN, NO 2, N 3, CHO, C 2-C 5Alkyl-carbonyl, C 2-C 5Carbalkoxy, C 2-C 4Alkyl amino-carbonyl, C 3-C 9Dialkyl amino carbonyl, the benzoyl that is replaced by Z arbitrarily, amino thiocarbonyl, C 1-C 4Alkylthio, C 1-C 4Alkyl sulphinyl, C 1-C 4Alkyl sulphonyl, the thiophenyl that is replaced by Z arbitrarily, the benzenesulfinyl that is replaced by Z arbitrarily, the benzenesulfonyl that is replaced by Z arbitrarily ,-P (=O) T 2T 3, or-P (=S) T 2T 3
[8] ethene derivatives of above-mentioned [4], wherein Q is the phenyl that is replaced by G arbitrarily, is replaced the De oxazolyl by R arbitrarily, arbitrarily the thiazolyl that is replaced by R, the pyrazolyl that is replaced by R arbitrarily, arbitrarily by R replace 1,2, the 3-triazolyl, the pyridyl that is replaced by R, or the pyrimidyl that is replaced by R arbitrarily arbitrarily.
[9] ethene derivatives of above-mentioned [8], wherein Q is the phenyl that is replaced by G arbitrarily.
[10] ethene derivatives of above-mentioned [8], wherein Q is replaced the De oxazolyl by R arbitrarily, or the 1,2,3-triazoles base that is replaced by R arbitrarily.
[11] ethene derivatives of above-mentioned [8], wherein Q is the thiazolyl that is replaced by R arbitrarily.
[12] ethene derivatives of above-mentioned [8], wherein Q is the pyrazolyl that is replaced by R arbitrarily.
[13] ethene derivatives of above-mentioned [5], wherein Q is the phenyl that is replaced by G arbitrarily, or Q-9, Q-10, Q-11, Q-12, Q-13, Q-14, Q-25, Q-26, Q-27, Q-28, Q-29, Q-30, Q-44, Q-45, Q-46, Q-47, Q-52, Q-53, Q-54, Q-55, Q-56 or Q-57.
[14] ethene derivatives of above-mentioned [7], wherein Q is the phenyl that is replaced by G arbitrarily, or Q-9, Q-10, Q-11, Q-12, Q-13, Q-14, Q-25, Q-26, Q-27, Q-28, Q-29, Q-30, Q-44, Q-45, Q-46, Q-47, Q-52, Q-53, Q-54, Q-55, Q-56 or Q-57.
[15] ethene derivatives of above-mentioned [13], wherein Q is Q-10, Q-44, Q-45, Q-46 or Q-47.
[16] ethene derivatives of above-mentioned [13], wherein Q is Q-12, Q-13 or Q-14.
[17] ethene derivatives of above-mentioned [13], wherein Q is Q-25, Q-26, Q-27, Q-28, Q-29 or Q-30.
[18] ethene derivatives of above-mentioned [13], wherein Q is the phenyl that is replaced by G arbitrarily.
[19] ethene derivatives of above-mentioned [2], wherein A is the phenyl that is replaced by W arbitrarily, the thiazolyl that is replaced by Y arbitrarily, the pyrazolyl that is replaced by Y arbitrarily, the pyridyl that is replaced by Y, or the pyrimidyl that is replaced by Y arbitrarily arbitrarily.
[20] above-mentioned ethene derivatives [3], wherein:
Q is the phenyl that is replaced by G arbitrarily, naphthyl, and Q-31, Q-32, Q-33, Q-34, Q-35, Q-36, Q-37, Q-44, Q-45, Q-46, Q-49,
Figure C9719404100351
Or
Figure C9719404100353
A is
Figure C9719404100361
Or
Y 2Be halogen atom, C 1-C 4Alkyl, C 1-C 4Haloalkyl, C 1-C 4Alkoxyl group, NO 2, CN, or C 2-C 5Carbalkoxy; And
Y 3Be halogen atom, C 1-C 4Alkyl, C 1-C 6Haloalkyl, C 2-C 4Alkoxyalkyl, or the phenyl that is replaced by X arbitrarily.
[21] ethene derivatives of above-mentioned [20], wherein E is CN.
[22] ethene derivatives of above-mentioned [20], wherein E is arbitrarily by C 1-C 4Alkyl or C 1-C 4The heterocyclic radical that haloalkyl replaces (described heterocyclic radical is 2-oxazolyl, 2-thiazolyl, 2-imidazolyl, 1,2,4-triazole-3-base, 1,2,4-oxadiazole-3-base, 1,2,4-thiadiazoles-3-base or 1,3,4-oxadiazole-2-yl), or halogen atom, C 2-C 4Alkynyl, the phenylacetylene base that is replaced by Z arbitrarily, C 1-C 4Haloalkyl, CN, NO 2, N 3, CHO, C 2-C 5Alkyl-carbonyl, C 2-C 5Carbalkoxy, C 2-C 4Alkyl amino-carbonyl, C 3-C 9Dialkyl amino carbonyl, the benzoyl that is replaced by Z arbitrarily, amino thiocarbonyl, C 1-C 4Alkylthio, C 1-C 4Alkyl sulphinyl, C 1-C 4Alkyl sulphonyl, the thiophenyl that is replaced by Z arbitrarily, the phenyl sulfinyl that is replaced by Z arbitrarily, the benzenesulfonyl that is replaced by Z arbitrarily ,-P (=O) T 2T 3, or-P (=S) T 2T 3
[23] ethene derivatives of above-mentioned [1], described derivative is selected from:
Or
Figure C9719404100401
[24] agricultural chemicals, described agricultural chemicals comprise one or more above-mentioned [1] to [23] ethene derivatives as activeconstituents.
[25] hydrobiont adheres to and prevents agent, describedly prevents that agent from containing the acrylonitrile derivative as one or more above-mentioned [1] to [23] of activeconstituents.
The compounds of this invention (I)-C (E)=C (OB)-fragment comprises two kinds of isomer: E-type and Z-type, these two kinds of isomer are all within the scope of the present invention.
Be appreciated that when substituent B is hydrogen atom formula of the present invention (I) compound exists with tautomeric forms as follows:
Although compound (I) exists with enol-type (1 ') basically,, under certain conditions, also can exist with tautomeric forms (2).The present invention should be interpreted as and comprise all these three kinds of tautomers and composition thereof.
Now, Q, A, B, E, G, R, R 1, Y, Y 1, Y 2, W, X, Z, T 1, T 2, T 3, T 4, T 5, T 6, T 7, Y 8, U 1, U 2, m, n, the preferred implementation of p and q is listed below.
The heterocyclic radical that is used for Q, A and B is represented following implication:
Specifically, thienyl is thiophene-2-base or thiene-3-yl-; Furyl is furans-2-base or furans-3-base; Pyrryl is pyrroles-1-base, pyrroles-2-base or pyrroles-3-base; Oxazolyl Shi oxazole-2-Ji ， oxazole-3-Ji ， oxazole-4-Ji Huo oxazole-5-base; Thiazolyl is a thiazol-2-yl, thiazole-4-base or thiazole-5-base; Imidazolyl is imidazoles-1-base, imidazoles-2-base or imidazol-4 yl; Isoxazolyl Shi isoxazole-3-base ， isoxazole-4-base Huo isoxazole-5-base; Isothiazolyl is isothiazole-3-base, isothiazole-4-base or isothiazole-5-base; Pyrazolyl is a pyrazol-1-yl, pyrazole-3-yl, pyrazoles-4-base or pyrazoles-5-base; 1,3,4-oxadiazole base is 1,3,4-oxadiazole-2 base; 1,3, the 4-thiadiazolyl group is 1,3,4-thiadiazoles-2-base; 1,2,4-oxadiazole base is 1,2,4-oxadiazole-3-base or 1,2,4-oxadiazole-5-base; 1,2, the 4-thiadiazolyl group is 1,2,4-thiadiazoles-3 base or 1,2,4-thiadiazoles-5-base; 1,2, the 4-triazolyl is 1,2,4-triazol-1-yl, 1,2,4-triazole-3-base or 1,2,4-triazole-4-base; 1,2, the 3-thiadiazolyl group is 1,2,3-thiadiazoles-4-base or 1,2,3-thiadiazoles-5-base; The 1,2,3-triazoles base is 1,2,3-triazoles-1-base, 1,2,3-triazoles-2-base or 1,2,3-triazoles-4-base; The pyrrotriazole base is pyrrotriazole-1-base, pyrrotriazole-2-base or pyrrotriazole-5-base; Pyridyl is pyridine-2-base, pyridin-3-yl or pyridin-4-yl; Pyrimidyl is a pyrimidine-2-base, pyrimidine-4-base or pyrimidine-5-base; Pyrazinyl pyrazine-2-base; Pyridazinyl is pyridazine-3-base or pyridazine-4-base; The 1,3,5-triazines base is 1,3,5-triazines-2-base; 1,2, the 4-triazinyl is 1,2,4-triazine-3-base, 1,2,4-triazine-5-base or 1,2,4-triazine-6-base; 1,2,4,5-tetrazine base is 1,2,4,5-tetrazine-3-base; Pyrazolinyl is 3-pyrazoline-1-base, 3-pyrazoline-3-base, 3-pyrazoline 4-base or 3-pyrazoline 5-base; Imidazolinyl is 1-tetrahydroglyoxaline-3-base, 1-tetrahydroglyoxaline-2-base, 1-tetrahydroglyoxaline-4-base or 4-tetrahydroglyoxaline-2-base; Oxazolinyl is 2-oxazoline-2-base, 2-oxazoline-4-base or 2-oxazoline-5-base; Isoxazoline-3-yl is 2-isoxazoline-3-base, 2-isoxazoline-4-base or 2-isoxazoline-5-base; Thiazolinyl 2-thiazoline-2-base, 2-thiazoline-4-base or 3-thiazoline-2-base; Imidazolidinonyl is imidazolidin-2-one-1-base; The tetrahydroglyoxaline ketone group is 2-imidazolone-1-base; And 3 (2H)-pyridazine ketone group be 3 (2H)-pyridazinone-2-base, 3 (2H)-pyridazinone-4-base, 3 (2H)-pyridazinone-5-base or 3 (2H)-pyridazinone-6-base.
The preferable range of Q is as follows:
QI: phenyl, thienyl, furyl, pyrryl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, pyrazolyl, imidazolyl, 1,3,4-oxadiazole base, 1,2,4-oxadiazole base, 1,3,4-thiadiazolyl group, 1,2,4-thiadiazolyl group, 1,2,4-triazolyl, 1,2,3-thiadiazolyl group, 1,2,3-triazolyl, 1,2,3,4-tetrazyl, pyridyl, pyrimidyl, pyrazinyl, pyridazinyl, 1,3,5-triazines base, 1,2,4-triazinyl, 1,2,4,5-tetrazine base.
QII: phenyl, thienyl, furyl, pyrryl, oxazolyl, isoxazolyl, thiazolyl, pyrazolyl, imidazolyl, 1,3,4-oxadiazole base, 1,2,4-oxadiazole base, 1,2,4-thiadiazolyl group, 1,2,4-triazolyl, 1,2,3-triazolyl, 1,2,3,4-tetrazyl, pyridyl, pyrimidyl.
QIII: phenyl, thienyl, oxazolyl, thiazolyl, pyrazolyl, pyridyl, pyrimidyl, 1,2,3-triazoles base.
QIV: phenyl.
QV: oxazolyl.
QVI: tetrazyl.
QVII: pyrazolyl.
QVIII: pyrimidyl.
QIX:1,2, the 3-triazolyl.
The preferable range of A is as follows:
AI: phenyl, thienyl, furyl, pyrryl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, pyrazolyl, imidazolyl, 1,3,4-oxadiazole base, 1,2,4-oxadiazole base, 1,3,4-thiadiazolyl group, 1,2,4-thiadiazolyl group, 1,2,4-triazolyl, 1,2,3-thiadiazolyl group, 1,2,3-triazoles base, 1,2,3,4-tetrazyl, pyridyl, pyrimidyl, pyrazinyl, pyridazinyl, 1,3,5-triazinyl, 1,2, the 4-triazinyl.
AII: phenyl, thienyl, furyl, pyrryl, oxazolyl, isoxazolyl, thiazolyl, pyrazolyl, imidazolyl, 1,2,3-triazoles base, 1,2,3-thiadiazolyl group, pyridyl, pyrimidyl, pyrazinyl, pyridazinyl.
AIII: phenyl, thiazolyl, pyrazolyl, pyridyl, pyrimidyl.
AIV: thiazolyl, pyrazolyl, pyridyl.
AV: thiazolyl.
AVI: pyrazolyl.
AVII: pyridyl.
The preferable range of B is as follows:
BI:H, C 1-C 4Alkyl, C 1-C 4Haloalkyl, C 2-C 4Alkoxyalkyl, CH 3OC 2H 4OCH 2, C 1-C 4Alkyl sulphonyl is arbitrarily by halogen or C 1-C 4The benzenesulfonyl that alkyl replaces ,-SO 2CF 3, C 2-C 8Dialkyl amino sulfonyl, C 3-C 9The dialkyl amido thiocarbonyl, C 3-C 9Alkoxy carbonyl alkyl ,-C (=O) T 1,-P (=O) T 2T 3,-P (=S) T 2T 3, basic metal, alkaline-earth metal or NHT 4T 5T 6
BII:H, C 1-C 4Alkyl, C 1-C 4Haloalkyl, C 2-C 4Alkoxyalkyl, CH 3OC 2H 4OCH 2, C 1-C 4Alkyl sulphonyl ,-SO 2CF 3,-C (=O) T 1, basic metal, alkaline-earth metal or NHT 4T 5T 6
BIII:H, C 2-C 4Alkoxyalkyl, C 1-C 4Alkyl sulphonyl ,-SO 2CF 3,-C (=O) T 1, basic metal, alkaline-earth metal or NHT 4T 5T 6
BIV:C 2-C 4Alkoxyalkyl, C 1-C 4Alkyl sulphonyl ,-SO 2CF 3,-C (=O) T 1, basic metal, alkaline-earth metal or NHT 4T 5T 6
The preferable range of E is as follows:
EI: halogen atom, C 2-C 4Alkynyl, the phenylacetylene base that is replaced by Z arbitrarily, C 1-C 4Haloalkyl, CN, NO 2, N 3, CHO, C 2-C 5Alkyl-carbonyl, C 2-C 5Carbalkoxy, C 2-C 4Alkyl amino-carbonyl, C 3-C 9Dialkyl amino carbonyl, the benzoyl that is replaced by Z arbitrarily, amino thiocarbonyl, C 1-C 4Alkylthio, C 1-C 4Alkyl sulphinyl, C 1-C 4Alkyl sulphonyl, the thiophenyl that is replaced by Z arbitrarily, the benzenesulfinyl that is replaced by Z arbitrarily, the benzenesulfonyl that is replaced by Z arbitrarily ,-P (=O) T 2T 3, or-P (=S) T 2T 3
EII: halogen atom, C 2-C 4Alkynyl, the phenylacetylene base that is replaced by Z arbitrarily, CN, C 2-C 5Alkyl-carbonyl, C 2-C 5Carbalkoxy, C 2-C 4Alkyl amino-carbonyl, C 3-C 9Dialkyl amino carbonyl, the benzoyl that is replaced by Z arbitrarily, amino thiocarbonyl, C 1-C 4Alkylthio, C 1-C 4Alkyl sulphinyl, C 1-C 4Alkyl sulphonyl, the thiophenyl that is replaced by Z arbitrarily, the benzenesulfinyl that is replaced by Z arbitrarily, arbitrarily the benzenesulfonyl that is replaced by Z or-P (=O) T 2T 3
EIII：CN。
The preferable range of G is as follows:
GI: substituting group freely is selected from: halogen atom, C 1-C 6Alkyl, C 2-C 4Alkenyl, C 2-C 4Alkynyl, C 1-C 4Haloalkyl, C 2-C 4Halogenated alkenyl, C 2-C 4The halo alkynyl is arbitrarily by C 1-C 3The C that alkyl replaces 3-C 6Cycloalkyl, C 1-C 6Alkoxyl group, C 2-C 4Alkenyloxy, C 2-C 4Alkynyloxy group, C 1-C 4Halogenated alkoxy, C 2-C 4The halo alkenyloxy, C 2-C 4The halo alkynyloxy group, C 1-C 4Alkylthio, C 1-C 4Alkyl sulphinyl, C 1-C 4Alkyl sulphonyl, C 2-C 4Alkenyl thio, C 2-C 4The alkenyl sulfinyl, C 2-C 4The alkenyl alkylsulfonyl, C 2-C 4The alkynes sulfenyl, C 2-C 4The alkynyl sulfinyl, C 2-C 4The alkynyl alkylsulfonyl, C 1-C 4Halogenated alkylthio, C 1-C 4The haloalkyl sulfinyl, C 1-C 4Halogenated alkyl sulfonyl, C 2-C 4The halo alkenyl thio, C 2-C 4The halogenated alkenyl sulfinyl, C 2-C 4The halogenated alkenyl alkylsulfonyl, C 2-C 4The acetylenic halide sulfenyl, C 2-C 4Halo alkynyl sulfinyl, C 2-C 4Halo alkynyl alkylsulfonyl, NO 2, CN ,-NU 1U 2, the methoxyl group that is replaced by phenyl, and described phenyl is arbitrarily by halogen or C 1-C 4Alkyl replaces, C 2-C 6Carbalkoxy, C 2-C 4Alkoxyalkyl, C 2-C 4Alkyl-carbonyl, C 2-C 4Halogenated alkyl carbonyl, C 2-C 5Alkyl carbonyl oxy, C 2-C 5Haloalkyl carbonyl oxygen base, C 3-C 7Dialkyl amido carbonyl oxygen base, the phenyl that is replaced by Z arbitrarily, the phenoxy group that is replaced by Z arbitrarily, the benzoyl that is replaced by Z arbitrarily, (condition is when substituting group is two or more for pyridyl that is replaced by Z and the pyridyloxy that is replaced by Z arbitrarily arbitrarily, described substituting group can be identical or different), and the quantity of substituting group G is 1,2,3 or 4; Or G is bonded on adjacent the position of substitution to form the alkylidene group of 5,6,7 or 8 yuan of rings.
GII: substituting group freely is selected from: halogen atom, C 1-C 6Alkyl, C 2-C 4Alkenyl, C 2-C 4Alkynyl, C 1-C 4Haloalkyl is arbitrarily by C 1-C 3The C that alkyl replaces 3-C 6Cycloalkyl, C 1-C 6Alkoxyl group, C 2-C 4Alkenyloxy, C 2-C 4Alkynyloxy group, C 1-C 4Halogenated alkoxy, C 2-C 4The halo alkenyloxy, C 1-C 4Alkylthio, C 1-C 4Alkyl sulphinyl, C 1-C 4Alkyl sulphonyl, C 2-C 4Alkenyl thio, C 2-C 4The alkenyl sulfinyl, C 2-C 4The alkenyl alkylsulfonyl, C 2-C 4The alkynes sulfenyl, C 2-C 4The alkynyl sulfinyl, C 2-C 4The alkynyl alkylsulfonyl, C 1-C 4Halogenated alkylthio, C 1-C 4The haloalkyl sulfinyl, C 1-C 4Halogenated alkyl sulfonyl, C 2-C 4The halo alkenyl thio, C 2-C 4The halogenated alkenyl sulfinyl, C 2-C 4The halogenated alkenyl alkylsulfonyl, the methoxyl group that is replaced by phenyl, and described phenyl is arbitrarily by halogen or C 1-C 4Alkyl replaces, C 2-C 6Carbalkoxy, C 2-C 5Alkyl carbonyl oxy, C 2-C 5Haloalkyl carbonyl oxygen base, phenoxy group that is replaced by Z and the pyridyloxy (condition is when substituting group is two or more, and described substituting group can be identical or different) that is replaced by Z arbitrarily arbitrarily, and the quantity of substituting group G is 1,2 or 3.
GIII: substituting group freely is selected from: halogen atom, C 1-C 6Alkyl, C 1-C 4Haloalkyl is arbitrarily by C 1-C 3The C that alkyl replaces 3-C 6Cycloalkyl, C 1-C 6Alkoxyl group, C 2-C 4Alkenyloxy, C 2-C 4Alkynyloxy group, C 1-C 4Halogenated alkoxy, C 2-C 4The halo alkenyloxy, C 1-C 4Alkylthio, C 1-C 4Alkyl sulphinyl, C 1-C 4Alkyl sulphonyl, C 2-C 4Alkenyl thio, C 2-C 4The alkenyl sulfinyl, C 2-C 4The alkenyl alkylsulfonyl, C 2-C 4The alkynes sulfenyl, C 2-C 4The alkynyl sulfinyl, C 2-C 4The alkynyl alkylsulfonyl, C 1-C 4Halogenated alkylthio, C 1-C 4The haloalkyl sulfinyl, C 1-C 4Halogenated alkyl sulfonyl, C 2-C 4The halo alkenyl thio, C 2-C 4The halogenated alkenyl sulfinyl, C 2-C 4The halogenated alkenyl alkylsulfonyl, the methoxyl group that is replaced by phenyl, and described phenyl is arbitrarily by halogen or C 1-C 4Alkyl replaces, C 2-C 6Carbalkoxy, C 2-C 5Alkyl carbonyl oxy, phenoxy group that is replaced by Z and the pyridyloxy (condition is when substituting group is two or more, and described substituting group can be identical or different) that is replaced by Z arbitrarily arbitrarily, and the quantity of substituting group G is 1 or 2.
The preferable range of R is as follows:
RI: substituting group freely is selected from: halogen atom, C 1-C 6Alkyl, the C that is replaced by phenyl 1-C 3Alkyl, and described phenyl is arbitrarily by halogen or C 1-C 4Alkyl replaces, C 1-C 6Haloalkyl is arbitrarily by C 1-C 3The C that alkyl replaces 3-C 6Cycloalkyl, C 1-C 4Alkoxyl group, C 2-C 4Alkenyloxy, C 2-C 4Alkynyloxy group, C 1-C 4Halogenated alkoxy, C 2-C 4The halo alkenyloxy, C 2-C 4The halo alkynyloxy group, C 1-C 4Alkylthio, C 1-C 4Alkyl sulphinyl, C 1-C 4Alkyl sulphonyl, C 2-C 4Alkenyl thio, C 2-C 4The alkenyl sulfinyl, C 2-C 4The alkenyl alkylsulfonyl, C 2-C 4The alkynes sulfenyl, C 2-C 4The alkynyl sulfinyl, C 2-C 4The alkynyl alkylsulfonyl, C 1-C 4Halogenated alkylthio, C 1-C 4The haloalkyl sulfinyl, C 1-C 4Halogenated alkyl sulfonyl, C 2-C 4The halo alkenyl thio, C 2-C 4The halogenated alkenyl sulfinyl, C 2-C 4The halogenated alkenyl alkylsulfonyl, NO 2, CN ,-NU 1U 2, naphthyl, C 2-C 4Carbalkoxy, C 2-C 4Alkoxyalkyl, the phenyl that is replaced by X arbitrarily, pyridyl that is replaced by X and the thienyl (condition is when substituting group is two or more, and described substituting group can be identical or different) that is replaced by X arbitrarily arbitrarily, and the quantity of substituent R is 1,2 or 3; Or R is bonded on adjacent the position of substitution to form the alkylidene group of 5,6,7 or 8 yuan of rings.
RII: substituting group freely is selected from: halogen atom, C 1-C 6Alkyl, the C that is replaced by phenyl 1-C 3Alkyl, and described phenyl is arbitrarily by halogen or C 1-C 4Alkyl replaces, C 1-C 4Haloalkyl is arbitrarily by C 1-C 3The C that alkyl replaces 3-C 6Cycloalkyl, NO 2, CN ,-NU 1U 2, naphthyl, C 2-C 4Carbalkoxy, C 2-C 4Alkoxyalkyl, phenyl that is replaced by X and the pyridyl (condition is when substituting group is two or more, and described substituting group can be identical or different) that is replaced by X arbitrarily arbitrarily, and the quantity of substituent R is 1,2 or 3.
RIII: freely be selected from: halogen atom, C 1-C 6Alkyl, the C that is replaced by phenyl 1-C 3Alkyl, and described phenyl is arbitrarily by halogen or C 1-C 4Alkyl replaces, C 1-C 4Haloalkyl is arbitrarily by C 1-C 3The C that alkyl replaces 3-C 6Cycloalkyl, NO 2, CN ,-NU 1U 2, naphthyl, C 2-C 4Carbalkoxy, phenyl that is replaced by X and the pyridyl (condition is when substituting group is two or more, and described substituting group can be identical or different) that is replaced by X arbitrarily arbitrarily, and the quantity of substituent R is 1 or 2.
According to by the difference of the heterocyclic radical type that R replaced, the quantity of R is also different.For 1,3,4-oxadiazole base, 1,2,4-oxadiazole base, 1,3,4-thiadiazolyl group, 1,2,4-thiadiazolyl group, 1,2,3-oxadiazole base, 1,2,3-thiadiazolyl group or pyrrotriazole base, the quantity of R is 0 or 1, preferred 1.For thiazolyl, oxazolyl, isoxazolyl, isothiazolyl, 1,3,4-triazolyl, 1,2,4-triazolyl, 1,2,3-triazoles base, 1,3,5-triazines base, 1,2,4-triazinyl or 1,2, the 4-triazinyl, the quantity of R is from 0 to 2 integer, preferred 1 or 2.For thienyl, furyl, pyrazolyl, imidazolyl, pyrimidyl, pyrazinyl or pyridazinyl, the quantity of R is from 0 to 3 integer, preferred from 0 to 2 integer, more preferably 1 or 2.For pyrryl, pyridyl, pyrazolinyl, imidazolinyl, oxazolinyl, isoxazoline-3-yl or thiazolinyl, the quantity of R is from 0 to 4 integer, preferred from 0 to 3 integer, more preferably 1 or 2.
The preferable range of Y is as follows:
YI: substituting group freely is selected from: halogen atom, C 1-C 6Alkyl, C 1-C 4Haloalkyl, C 1-C 4Alkoxyl group, C 2-C 4Alkenyloxy, C 2-C 4Alkynyloxy group, C 1-C 4Halogenated alkoxy, C 2-C 4The halo alkenyloxy, C 2-C 4The halo alkynyloxy group, C 1-C 4Alkylthio, C 1-C 4Alkyl sulphinyl, C 1-C 4Alkyl sulphonyl, C 2-C 4Alkenyl thio, C 2-C 4The alkenyl sulfinyl, C 2-C 4The alkenyl alkylsulfonyl, C 2-C 4The alkynes sulfenyl, C 2-C 4The alkynyl sulfinyl, C 2-C 4The alkynyl alkylsulfonyl, C 1-C 4Halogenated alkylthio, C 1-C 4The haloalkyl sulfinyl, C 1-C 4Halogenated alkyl sulfonyl, C 2-C 4The halo alkenyl thio, C 2-C 4The halogenated alkenyl sulfinyl, C 2-C 4The halogenated alkenyl alkylsulfonyl, C 2-C 4The acetylenic halide sulfenyl, C 2-C 4Halo alkynyl sulfinyl, C 2-C 4Halo alkynyl alkylsulfonyl, NO 2, CN ,-NU 1U 2, C 2-C 4Carbalkoxy, C 2-C 4Alkoxyalkyl, C 2-C 4Alkyl carbonyl oxy, C 2-C 4Haloalkyl carbonyl oxygen base and the phenyl (condition is when substituting group is two or more, and described substituting group can be identical or different) that is replaced by X arbitrarily, and the quantity of substituting group Y is 1,2 or 3.
YII: substituting group freely is selected from: halogen atom, C 1-C 4Alkyl, C 1-C 4Haloalkyl, C 1-C 4Alkoxyl group, C 1-C 4Alkylthio, C 1-C 4Alkyl sulphinyl, C 1-C 4Alkyl sulphonyl, C 1-C 4Halogenated alkylthio, C 1-C 4The haloalkyl sulfinyl, C 1-C 4Halogenated alkyl sulfonyl, NO 2, CN, C 2-C 4Carbalkoxy and the phenyl (condition is when substituting group is two or more, and described substituting group can be identical or different) that is replaced by X arbitrarily, and the quantity of substituting group Y is 1,2 or 3.
According to by the difference of the heterocyclic radical type that Y replaced, the quantity of Y is also different.For 1,3,4-oxadiazole base, 1,2,4-oxadiazole base, 1,3,4-thiadiazolyl group, 1,2,4-thiadiazolyl group, 1,2,3-thiadiazolyl group or pyrrotriazole base, the quantity of R is 0 or 1, preferred 1.For thiazolyl, oxazolyl, isoxazolyl, isothiazolyl, 1,3,4-triazolyl, 1,2,4-triazolyl, 1,2,3-triazoles base, 1,3,5-triazines base, 1,2,4-triazinyl or 1,2, the 4-triazinyl, the quantity of R is from 0 to 2 integer, preferred 1 or 2.For thienyl, furyl, pyrazolyl, imidazolyl, pyrimidyl, pyrazinyl or pyridazinyl, the quantity of R is from 0 to 3 integer, preferred from 0 to 2 integer, more preferably 1 or 2.For pyrryl, pyridyl, pyrazolinyl, imidazolinyl, oxazolinyl, isoxazoline-3-yl or thiazolinyl, the quantity of R is from 0 to 4 integer, preferred from 0 to 3 integer, more preferably 1 or 2.
The preferable range of W is as follows:
WI: substituting group freely is selected from: halogen atom, C 1-C 6Alkyl, C 1-C 4Haloalkyl, C 1-C 4Alkoxyl group, C 1-C 4Halogenated alkoxy, C 1-C 4Alkylthio, C 1-C 4Alkyl sulphinyl, C 1-C 4Alkyl sulphonyl, C 1-C 4Halogenated alkylthio, C 1-C 4The haloalkyl sulfinyl, C 1-C 4Halogenated alkyl sulfonyl, C 2-C 4Alkenyloxy, C 2-C 4The halo alkenyloxy, C 2-C 4Alkenyl thio, C 2-C 4The alkenyl sulfinyl, C 2-C 4The alkenyl alkylsulfonyl, C 2-C 4The halo alkenyl thio, C 2-C 4The halogenated alkenyl sulfinyl, C 2-C 4The halogenated alkenyl alkylsulfonyl, C 2-C 4Alkynyloxy group, C 2-C 4The alkynes sulfenyl, C 2-C 4The alkynyl sulfinyl, C 2-C 4The alkynyl alkylsulfonyl, NO 2, CN, C 2-C 4Carbalkoxy, C 2-C 4Alkyl-carbonyl, C 2-C 4Haloalkyl carbonyl oxygen base, C 2-C 4Alkyl carbonyl oxy and-NU 1U 2(condition is when substituting group is two or more, and described substituting group can be identical or different), and the quantity of substituting group W is 1,2,3 or 4.
WII: substituting group freely is selected from: halogen, C 1-C 4Alkyl, C 1-C 4Haloalkyl, C 1-C 4Alkoxyl group, C 1-C 4Halogenated alkoxy, C 1-C 4Alkylthio, C 1-C 4Alkyl sulphinyl, C 1-C 4Alkyl sulphonyl, C 1-C 4Halogenated alkylthio, C 1-C 4The haloalkyl sulfinyl, C 1-C 4Halogenated alkyl sulfonyl, C 2-C 4Alkenyloxy, C 2-C 4The halo alkenyloxy, C 2-C 4Alkenyl thio, C 2-C 4The alkenyl sulfinyl, C 2-C 4The alkenyl alkylsulfonyl, C 2-C 4Alkynyloxy group, C 2-C 4The alkynes sulfenyl, C 2-C 4The alkynyl sulfinyl, C 2-C 4The alkynyl alkylsulfonyl, NO 2And CN (condition is when substituting group is two or more, and described substituting group can be identical or different), and the quantity of substituting group W is 1,2 or 3.
WIII: substituting group freely is selected from: halogen, C 1-C 4Alkyl, C 1-C 4Haloalkyl, C 1-C 4Alkoxyl group, C 1-C 4Halogenated alkoxy, C 1-C 4Alkylthio, C 1-C 4Alkyl sulphinyl, C 1-C 4Alkyl sulphonyl, C 1-C 4Halogenated alkylthio, C 1-C 4The haloalkyl sulfinyl, C 1-C 4Halogenated alkyl sulfonyl, NO 2And CN (condition is when substituting group is two or more, and described substituting group can be identical or different), and the quantity of substituting group W is 1 or 2.
T 1Preferable range as follows:
T 1I:C 1-C 18Alkyl, C 2-C 6Alkenyl, C 1-C 4Haloalkyl, C 1-C 4Alkoxy-C 1-C 4Alkyl, the C that is replaced by phenyl 1-C 4Alkyl, and described phenyl is arbitrarily by halogen or C 1-C 4Alkyl replaces, C 3-C 6Halogenated cycloalkyl is arbitrarily by C 1-C 3The C that alkyl replaces 3-C 6Cycloalkyl, the cycloalkyl that is replaced by phenyl, and described phenyl is arbitrarily by halogen or C 1-C 4Alkyl replaces, the C that is replaced by phenyl 2-C 4Alkenyl, and described phenyl is arbitrarily by halogen or C 1-C 4Alkyl replaces, C 1-C 10Alkoxyl group, C 1-C 4Halogenated alkoxy, C 2-C 5Alkenyloxy is arbitrarily by C 1-C 3The C that alkyl replaces 3-C 6Cycloalkyloxy, benzyloxy, C 2-C 5Carbalkoxy ,-NU 1U 2, the phenyl that is replaced by Z, the phenoxy group that is replaced by Z arbitrarily arbitrarily, the thiophenyl that is replaced by Z arbitrarily, (described heterocyclic radical is selected from thienyl for naphthyl and the heterocyclic radical that replaced by Z arbitrarily, furyl, pyrryl oxazolyl isoxazolyl, thiazolyl, pyrazolyl, imidazolyl, 1,3,4-oxadiazole base, 1,2,4-oxadiazole base, 1,3, the 4-thiadiazolyl group, 1,2, the 4-thiadiazolyl group, 1,2, the 4-triazolyl, 1,2, the 3-thiadiazolyl group, 1,2, the 3-triazolyl, 1,2,3, the 4-tetrazyl, pyridyl, pyrimidyl, pyrazinyl, pyridazinyl, 1,3,5-triazines base and 1,2, the 4-triazinyl).
T 1II:C 1-C 18Alkyl, C 2-C 6Alkenyl, C 1-C 4Haloalkyl, C 2-C 4Alkoxyalkyl, the C that is replaced by phenyl 1-C 4Alkyl, and described phenyl is arbitrarily by halogen or C 1-C 4Alkyl replaces, arbitrarily by C 1-C 3The C that alkyl replaces 3-C 6Cycloalkyl, the cycloalkyl that is replaced by phenyl, and described phenyl is arbitrarily by halogen or C 1-C 4Alkyl replaces, the C that is replaced by phenyl 2-C 4Alkenyl, and described phenyl is arbitrarily by halogen or C 1-C 4Alkyl replaces, C 1-C 10Alkoxyl group, C 1-C 4Halogenated alkoxy, C 2-C 5Alkenyloxy, C 3-C 6Cycloalkyloxy, benzyloxy, C 2-C 5Carbalkoxy, the phenyl that is replaced by Z, the phenoxy group that is replaced by Z, thiophenyl, naphthyl and the heterocyclic radical (described heterocyclic radical is selected from thienyl, furyl, oxazolyl, thiazolyl, pyrazolyl and pyridyl) that is replaced by Z arbitrarily arbitrarily arbitrarily.
T 1III:C 1-C 17Alkyl, C 2-C 6Alkenyl, C 1-C 4Haloalkyl, C 2-C 4Alkoxyalkyl, the C that is replaced by phenyl 1-C 4Alkyl is arbitrarily by C 1-C 3The C that alkyl replaces 3-C 6Cycloalkyl, the cycloalkyl that is replaced by phenyl, the C that is replaced by phenyl 2-C 4Alkenyl, C 1-C 8Alkoxyl group, C 1-C 4Halogenated alkoxy, C 2-C 5Alkenyloxy, C 3-C 6Cycloalkyloxy, benzyloxy, C 2-C 5Carbalkoxy, the phenyl that is replaced by Z arbitrarily, the phenoxy group that is replaced by Z arbitrarily, thiophenyl, naphthyl, pyrazolyl that is replaced by Z or the pyridyl that is replaced by Z arbitrarily arbitrarily.
T 2Preferable range as follows:
T 2I: phenyl, C 1-C 4Alkyl, C 1-C 4Alkoxyl group or C 1-C 4Alkylthio.
T 3Preferable range as follows:
T 2I: phenyl, C 1-C 6Alkyl, C 1-C 6Alkoxyl group or C 1-C 4Alkylthio.
T 4Preferable range as follows:
T 4I:H, C 1-C 4Alkyl, C 3-C 6Cycloalkyl, or benzyl; T equally preferably 4, T 5And T 6In any two nitrogen-atoms with institute's bonding form 5,6 or 7 yuan of rings, and described ring contains aerobic, nitrogen and/or sulphur atom arbitrarily.
T 5Preferable range as follows:
T 5I:H, C 1-C 4Alkyl, C 3-C 6Cycloalkyl, or benzyl; T equally preferably 4, T 5And T 6In any two nitrogen-atoms with institute's bonding form 5,6 or 7 yuan of rings, and described ring contains aerobic, nitrogen and/or sulphur atom arbitrarily.
T 6Preferable range as follows:
T 6I:H, C 1-C 4Alkyl, C 3-C 6Cycloalkyl, or benzyl; T equally preferably 4, T 5And T 6In any two nitrogen-atoms with institute's bonding form 5,6 or 7 yuan of rings, and described ring contains aerobic, nitrogen and/or sulphur atom arbitrarily.
The preferable range of X is as follows:
XI: substituting group freely is selected from: halogen, C 1-C 4Alkyl, C 1-C 4Haloalkyl, C 1-C 4Alkoxyl group, C 1-C 4Halogenated alkoxy, C 1-C 4Alkylthio, C 1-C 4Alkyl sulphinyl, C 1-C 4Alkyl sulphonyl, C 2-C 5Alkenyl thio, C 2-C 5The alkenyl sulfinyl, C 2-C 5The alkenyl alkylsulfonyl, C 1-C 4Halogenated alkylthio, C 1-C 4The haloalkyl sulfinyl, C 1-C 4Halogenated alkyl sulfonyl, NO 2, CN ,-NU 1U 2And C 2-C 5Carbalkoxy (condition is when substituting group is two or more, and described substituting group can be identical or different), and the quantity of substituent X is 1,2 or 3.
XII: substituting group freely is selected from: halogen, C 1-C 4Alkyl, C 1-C 4Haloalkyl, C 1-C 4Alkoxyl group, C 1-C 4Halogenated alkoxy, C 1-C 4Alkylthio, C 1-C 4Alkyl sulphinyl, C 1-C 4Alkyl sulphonyl, C 2-C 5Alkenyl thio, C 1-C 4Halogenated alkylthio, C 1-C 4The haloalkyl sulfinyl, C 1-C 4Halogenated alkyl sulfonyl and NO 2(condition is when substituting group is two or more, and described substituting group can be identical or different), and the quantity of substituent X is 1,2 or 3.
XIII: substituting group freely is selected from: halogen, C 1-C 4Alkyl, C 1-C 4Haloalkyl and C 1-C 4Alkoxyl group (condition is when substituting group is two or more, and described substituting group can be identical or different), and the quantity of substituent X is 1 or 2.
According to by the difference of the lopps type that X replaced, the quantity of X is also different.For phenyl, the quantity of X is from 0 to 5 integer, preferably from 0 to 3 integer, more preferably from 0 to 2 integer.For pyridyl, the quantity of X is from 0 to 4 integer, and is preferred 0,1 or 2, more preferably 0 or 1.For thienyl, the quantity of X is from 0 to 3 integer, preferred 0 or 1.
The preferable range of Z is as follows:
ZI: freely be selected from: halogen, C 1-C 4Alkyl, C 1-C 4Haloalkyl, C 1-C 4Alkoxyl group, C 1-C 4Halogenated alkoxy, C 1-C 4Alkylthio, C 1-C 4Alkyl sulphinyl, C 1-C 4Alkyl sulphonyl, C 2-C 5Alkenyl thio, C 2-C 5The alkenyl sulfinyl, C 2-C 5The alkenyl alkylsulfonyl, C 1-C 4Halogenated alkylthio, C 1-C 4The haloalkyl sulfinyl, C 1-C 4Halogenated alkyl sulfonyl, NO 2, CN ,-NU 1U 2And C 2-C 5Carbalkoxy (condition is when substituting group is two or more, and described substituting group can be identical or different), and the quantity of substituting group Z is 1,2,3 or 4.
ZII: freely be selected from: halogen, C 1-C 4Alkyl, C 1-C 4Haloalkyl, C 1-C 4Alkoxyl group, C 1-C 4Halogenated alkoxy, C 1-C 4Alkylthio, C 1-C 4Alkyl sulphinyl, C 1-C 4Alkyl sulphonyl, C 2-C 5Alkenyl thio, C 2-C 5The alkenyl sulfinyl, C 2-C 5The alkenyl alkylsulfonyl, C 1-C 4Halogenated alkylthio, C 1-C 4Haloalkyl sulfinyl and C 1-C 4Halogenated alkyl sulfonyl (condition is when substituting group is two or more, and described substituting group can be identical or different), and the quantity of substituting group Z is 1,2,3 or 4.
According to by the difference of the lopps type that Z replaced, the quantity of Z is also different.For phenyl, the quantity of Z is from 0 to 5 integer, preferred from 0 to 4 integer, more preferably 0,1,2 or 3, most preferably 0,1 or 2.For naphthyl, the quantity of Z is from 0 to 7 integer, preferred 0.When the ring that is replaced by Z was heterocyclic radical, the quantity of substituting group Z is the difference with the difference of heterocyclic radical type equally.For 1,3,4-oxadiazole base, 1,2,4-oxadiazole base, 1,3,4-thiadiazolyl group, 1,2,4-thiadiazolyl group, 1,2,3-oxadiazole base, 1,2,3-thiadiazolyl group, pyrrotriazole base or 1,2,3, the 5-tetrazyl, the quantity of Z is 0 or 1.For thiazolyl, oxazolyl, isoxazolyl, isothiazolyl, 1,3,4-triazolyl, 1,2,4-triazolyl, 1,2,3-triazoles base, 1,3,5-triazines base, 1,2,4-triazinyl or 1,2, the 4-triazinyl, the quantity of Z is from 0 to 2 integer, preferred 1 or 2.For thienyl, furyl, pyrazolyl, imidazolyl, pyrimidyl, pyrazinyl or pyridazinyl, the quantity of Z is from 0 to 3 integer, preferred from 0 to 2 integer, more preferably 1 or 2.For pyrryl, pyridyl, pyrazolinyl, imidazolinyl, oxazolinyl, isoxazoline-3-yl or thiazolinyl, the quantity of Z is from 0 to 4 integer, preferred from 0 to 2 integer, more preferably 1 or 2.
T 7Preferable range as follows:
T 7I:H, phenyl, benzyl, or C 1-C 4Alkyl; T equally preferably 7And T 8Carbon atom with institute's bonding forms 5 yuan or 6 yuan of rings.
T 8Preferable range as follows:
T 8I:H, phenyl, benzyl, or C 1-C 4Alkyl; T equally preferably 7And T 8Carbon atom with institute's bonding forms 5 yuan or 6 yuan of rings.
U 1Preferable range as follows:
U 1I:H, C 1-C 4Alkyl or C 2-C 5Alkyl-carbonyl; U equally preferably 1And U 2Carbon atom with institute's bonding forms 5,6 or 7 yuan of rings.
U 2Preferable range as follows:
U 2I:H, C 1-C 4Alkyl or C 2-C 5Alkyl-carbonyl; U equally preferably 1And U 2Nitrogen-atoms with institute's bonding forms 5,6 or 7 yuan of rings.
M preferably 1,2 or 3, and more preferably 1 or 2.
N preferably 0,1,2 or 3, and more preferably 1 or 2.
P preferably 1 or 2.
More than in the preferred group combination arbitrarily described in the scope of preferred substituents, and demonstrate the scope of preferred compound of the present invention.Hereinafter should be mentioned that particularly preferred scope.
The compounds of this invention, this compound comprises preferred substituents QI, AI, BI, EI, GI, RI, YI, WI, T 1I, T 2I, T 3I, T 4I, T 5I, T 6I, XI, ZI, T 7I, T 8I, U 1I and U 2I.
The compounds of this invention, this compound comprises preferred substituents QI, AI, BI, EIII, GI, RI, YI, WI, T 1I, T 2I, T 3I, T 4I, T 5I, T 6I, XI, ZI, T 7I, T 8I, U 1I and U 2I.
The compounds of this invention, this compound comprises preferred substituents QII, AII, BI, EII, GI, RI, YI, WI, T 1I, T 2I, T 3I, T 4I, T 5I, T 6I, XI, ZI, T 7I, T 8I, U 1I and U 2I.
The compounds of this invention, this compound comprises preferred substituents QII, AII, BI, EIII, GI, RI, YI, WI, T 1I, T 2I, T 3I, T 4I, T 5I, T 6I, XI, ZI, T 7I, T 8I, U 1I and U 2I.
The compounds of this invention, this compound comprises preferred substituents QIII, AIII, BI, EIII, GI, RI, YI, WI, T 1I, T 2I, T 3I, T 4I, T 5I, T 6I, XI, ZI, T 7I, T 8I, U 1I and U 2I.
The compounds of this invention, this compound comprises preferred substituents QIII, AIII, BII, EIII, GII, RII, YII, WII, T 1II, T 2I, T 3I, T 4I, T 5I, T 6I, XII, ZII, T 7I, T 8I, U 1I and U 2I.
The compounds of this invention, this compound comprises preferred substituents QIII, AIII, BII, EIII, GIII, RIII, YII, WII, T 1III, T 2I, T 3I, T 4I, T 5I, T 6I, XIII, ZII, T 7I, T 8I, U 1I and U 2I.
The compounds of this invention, this compound comprises preferred substituents QIII, AIV, BIII, EIII, GIII, RIII, YII, WII, T 1III, T 2I, T 3I, T 4I, T 5I, T 6I, XIII, ZII, T 7I, T 8I, U 1I and U 2I.
The compounds of this invention, this compound comprises preferred substituents QIV, AIV, BIII, EIII, GIII, RIII, YII, WII, T 1III, T 2I, T 3I, T 4I, T 5I, T 6I, XIII, ZII, T 7I, T 8I, U 1I and U 2I.
The compounds of this invention, this compound comprises preferred substituents QV, AIII, BIII, EIII, GIII, RIII, YII, WII, T 1III, T 2I, T 3I, T 4I, T 5I, T 6I, XIII, ZII, T 7I, T 8I, U 1I and U 2I.
The compounds of this invention, this compound comprises preferred substituents QVI, AIII, BIII, EIII, GIII, RIII, YII, WII, T 1III, T 2I, T 3I, T 4I, T 5I, T 6I, XIII, ZII, T 7I, T 8I, U 1I and U 2I.
The compounds of this invention, this compound comprises preferred substituents QVI, AIV, BIII, EIII, GIII, RIII, YII, WII, T 1III, T 2I, T 3I, T 4I, T 5I, T 6I, XIII, ZII, T 7I, T 8I, U 1I and U 2I.
The compounds of this invention, this compound comprises preferred substituents QVII, AIII, BIII, EIII, GIII, RIII, YII, WII, T 1III, T 2I, T 3I, T 4I, T 5I, T 6I, XIII, ZII, T 7I, T 8I, U 1I and U 2I.
The compounds of this invention, this compound comprises preferred substituents QVIII, AIII, BIII, EIII, GIII, RIII, YII, WII, T 1III, T 2I, T 3I, T 4I, T 5I, T 6I, XIII, ZII, T 7I, T 8I, U 1I and U 2I.
The compounds of this invention, this compound comprises preferred substituents QIX, AIII, BIII, EIII, GIII, RIII, YII, WII, T 1III, T 2I, T 3I, T 4I, T 5I, T 6I, XIII, ZII, T 7I, T 8I, U 1I and U 2I.
The compounds of this invention, this compound comprises preferred substituents QIII, AV, BIII, EIII, GIII, RIII, YII, WII, T 1III, T 2I, T 3I, T 4I, T 5I, T 6I, XIII, ZII, T 7I, T 8I, U 1I and U 2I.
The compounds of this invention, this compound comprises preferred substituents QIII, AVI, BIII, EIII, GIII, RIII, YII, WII, T 1III, T 2I, T 3I, T 4I, T 5I, T 6I, XIII, ZII, T 7I, T 8I, U 1I and U 2I.
The compounds of this invention, this compound comprises preferred substituents QIII, AVII, BIII, EIII, GIII, RIII, YII, WII, T 1III, T 2I, T 3I, T 4I, T 5I, T 6I, XIII, ZII, T 7I, T 8I, U 1I and U 2I.
Now, Q, A, B, E, G, R, R 1, Y, Y 1, Y 2, W, X, Z, T 1, T 2, T 3, T 4, T 5, T 6, T 7, T 8, U 1And U 2Specific examples will be listed below.
E, G, R, R 1, W, X, Y, Y 1, Y 2, Y 3Comprise fluorine atom, chlorine atom, bromine atoms and iodine atom with the halogen atom among the Z.Preferred fluorine atom, chlorine atom and bromine atoms.
For B, G, R, R 1, T 1, T 2, T 3, T 4, T 5, T 6, T 7, T 8, U 1, U 2, W, X, Y, Y 1, Y 2, Y 3With alkyl among the Z can be to have the straight or branched alkyl of specifying carbonatoms, comprise: methyl for example, ethyl, n-propyl, sec.-propyl, normal-butyl, isobutyl-, the tertiary butyl, sec-butyl, penta-1-base, penta-2-base, penta-3-base, 2-methyl fourth-1-base, 2-methyl fourth-2-base, 2-methyl fourth-3-base, 3-methyl fourth-1-base, 2,2-dimethyl propylene-1-base, oneself-the 1-base, oneself-the 2-base, oneself-the 3-base, the 1-methyl amyl, the 2-methyl amyl, the 3-methyl amyl, the 4-methyl amyl, 1, the 1-dimethylbutyl, 1, the 2-dimethylbutyl, 1, the 3-dimethylbutyl, 2, the 2-dimethylbutyl, 2, the 3-dimethylbutyl, 3, the 3-dimethylbutyl, the 1-ethyl-butyl, the 2-ethyl-butyl, 1,1,2-trimethylammonium propyl group, 1,2,2-trimethylammonium propyl group, 1-ethyl-1-methyl-propyl, 1-ethyl-2-methyl-propyl, n-heptyl, n-octyl, n-nonyl, the n-undecane base, dodecyl, the n-tridecane base, the n-tetradecane base, the Pentadecane base, n-hexadecyl, the n-heptadecane base, the Octadecane base, NSC 77136 base and NSC 62789 base.
For G, R, R 1, T 1, T 4, T 5, T 6, Y 1With W, alkenyl can be to have the straight or branched alkenyl of specifying carbonatoms, comprise: vinyl for example, the 1-propenyl, the 2-propenyl, the 1-butylene base, crotyl, the 3-butenyl, 1-methyl-2-propenyl, 2-methyl-2-propenyl, 1-pentenyl pentenyl, the 3-pentenyl, the 4-pentenyl, 1-methyl-2-butene base, 2-methyl-2-butene base, 3-methyl-2-butene base, 1-methyl-3-butenyl, 2-methyl-3-butenyl, 3-methyl-3-butenyl, 1,1-dimethyl-2-propenyl, 1,2-dimethyl-2-propenyl, 1-ethyl-2-propenyl, the 1-hexenyl, the 2-hexenyl, the 3-hexenyl, the 4-hexenyl, the 5-hexenyl, 1-methyl-pentenyl, 2-methyl-pentenyl, 3-methyl-pentenyl, 4-methyl-pentenyl, 1-methyl-3-pentenyl, 2-methyl-3-pentenyl, 3-methyl-3-pentenyl, 4-methyl-3-pentenyl, 1-methyl-4-pentenyl, 2-methyl-4-pentenyl, 3-methyl-4-pentenyl, 4-methyl-4-pentenyl, 1,1-dimethyl-crotyl, 1,1-dimethyl-3-butenyl, 1,2-dimethyl-crotyl, 1,2-dimethyl-3-butenyl, 1,3-dimethyl-crotyl, 1,3-dimethyl-3-butenyl, 2,3-dimethyl-crotyl, 2,3-dimethyl-3-butenyl, 3,3-dimethyl-crotyl, 1-ethyl-crotyl, 1-ethyl-3-butenyl, 2-ethyl-crotyl, 2-ethyl-3-butenyl, 1,1,2-trimethylammonium-2-propenyl and 1-ethyl-1-methyl-2-propenyl.
For E, G, R, R 1, Y 1With W, alkynyl can be to have the straight or branched alkynyl of specifying carbonatoms, comprise: ethynyl for example, the 1-proyl, 2-propynyl, the ethyl acetylene base, the 2-butyne base, the 3-butynyl, 1-methyl-2-propynyl, the 1-pentynyl, the valerylene base, the 3-pentynyl, the 4-pentynyl, 1-methyl-2-butyne base, 1-methyl-3-butynyl, 2-methyl-3-butynyl, the hexin base, 1-methyl-3-pentynyl, 1-methyl-4-pentynyl, 2-methyl-3-pentynyl, 2-methyl-4-pentynyl, 3-methyl-4-pentynyl, 4-methyl-valerylene base, 1,1-dimethyl-2-butyne base, 1,1-dimethyl-3-butynyl, 1,2-dimethyl-3-butynyl, 2,2-dimethyl-3-butynyl, 1-ethyl-2-butyne base, 1-ethyl-3-butynyl and 2-ethyl-3-butynyl.
For B, E, G, R, R 1, T 1, W, X, Y, Y 1, Y 2, Y 3With Z, haloalkyl can be to have the straight or branched haloalkyl of specifying carbonatoms, comprising: for example methyl fluoride, chloromethyl, brooethyl, fluoro ethyl, chloroethyl, bromotrifluoromethane, fluoro n-propyl, chloro n-propyl, difluoromethyl, chloro difluoromethyl, trifluoromethyl, dichloromethyl, trichloromethyl, two fluoro ethyls, trifluoroethyl, three chloroethyls, chloro difluoromethyl, bromo difluoromethyl, trifluoro chloroethyl, hexafluoro n-propyl, chlorobutyl, fluorine butyl, chloro n-pentyl, fluoro n-pentyl, chloro n-hexyl and fluoro n-hexyl.
For G, R, T 1, T 4, T 5And T 6, any C that replaces 3-C 6Cycloalkyl comprises: for example cyclopropyl, 1-methyl cyclopropyl, 2,2,3,3-tetramethyl-ring propyl group, cyclobutyl, 1-ethyl cyclobutyl, 1-normal-butyl cyclobutyl, cyclopentyl, 1-methylcyclopentyl, cyclohexyl, 1-methylcyclohexyl and 4-methylcyclohexyl.
For B, G, R and R 1, the C that is replaced by phenyl 1-C 4(described phenyl is arbitrarily by halogen or C for alkyl 1-C 4Alkyl replaces) comprising: benzyl for example, 2-benzyl chloride base, the 3-bromobenzyl, 4-benzyl chloride base, the 4-methyl-benzyl, 4-tertiary butyl benzyl, the 1-phenylethyl, 1-(3-chloro-phenyl-) ethyl, the 2-phenylethyl, 1-methyl isophthalic acid-phenylethyl, 1-(4-chloro-phenyl-)-1-methylethyl, 1-(3-chloro-phenyl-)-1-methylethyl, the 1-phenyl propyl, the 2-phenyl propyl, the 3-phenyl propyl, the 1-phenyl propyl, the 2-phenyl butyl, the 3-phenyl butyl, the 4-phenyl butyl, 1-methyl isophthalic acid-phenyl propyl, 1-methyl-2-phenyl propyl, 1-methyl-3-phenyl propyl, 2-methyl-2-phenyl propyl, 2-(4-chloro-phenyl-)-2-methyl-propyl and 2-methyl-2-(3-aminomethyl phenyl) propyl group.
For T 1, the C that is replaced by phenyl 3-C 6(described phenyl is arbitrarily by halogen or C for cycloalkyl 1-C 4Alkyl replaces) comprising: 1-phenycyclopropyl for example, 1-(3-chloro-phenyl-) cyclopropyl, 1-(4-chloro-phenyl-) cyclopropyl, 1-(4-bromophenyl) cyclopropyl, 1-(4-fluorophenyl) cyclopropyl, 1-(4-ethylphenyl) cyclopropyl, 1-(4-propyl group phenyl) cyclopropyl, the 2-phenycyclopropyl, 1-benzyl ring butyl, 2-benzyl ring butyl, 1-benzyl ring amyl group, 1-(4-chloro-phenyl-) cyclopentyl, 2-benzyl ring amyl group, 3-benzyl ring amyl group, 1-benzyl ring hexyl, 1-(3-fluorophenyl) cyclohexyl, 1-(4-chloro-phenyl-) cyclohexyl, 1-(4-tert-butyl-phenyl) cyclohexyl, 2-benzyl ring hexyl, 3-benzyl ring hexyl and 4-benzyl ring hexyl.
For T 1, by phenyl and C 1-C 4(described phenyl is arbitrarily by halogen or C for the common cyclopropyl that replaces of alkyl 1-C 4Alkyl replaces) comprising: for example 2,2-dimethyl-1-phenycyclopropyl, 1-(4-chloro-phenyl-)-2,2-dimethyl cyclopropyl, 2,2-dimethyl-3-phenycyclopropyl, 3-(3-chloro-phenyl-)-2,2-dimethyl cyclopropyl, (4-chloro-phenyl-)-2,2-dimethyl-3-phenycyclopropyl, (4-bromophenyl)-2,2-dimethyl-3-phenycyclopropyl, 2,2-dimethyl-3-(4-aminomethyl phenyl) cyclopropyl and (4-tert-butyl-phenyl)-2,2-dimethyl-3-phenycyclopropyl.
For T 1, by the C of phenyl and halogen replacement 3-C 4(described phenyl is arbitrarily by halogen or C for cyclopropyl 1-C 4Alkoxyl group replaces) comprising: for example 2,2-two chloro-1-phenycyclopropyls, 2,2-two chloro-1-(3-chloro-phenyl-) cyclopropyl, 2,2-two chloro-1-(4-p-methoxy-phenyl) cyclopropyl, 2,2-two chloro-1-(4-ethoxyl phenenyl) cyclopropyl, 2,2-two chloro-(4-isopropyl phenyl) cyclopropyl, 2,2-two chloro-1-(4-tert-butyl-phenyl) cyclopropyl, 2,2-two chloro-1-(4-p-methoxy-phenyl)-3-phenycyclopropyl and 1-(4-ethoxyl phenenyl)-2,2,3,3-tetrafluoro butyl.
For T 1, by C 2-C 4Alkenyl and C 1-C 4The common cyclopropyl (described alkenyl is replaced by halogen arbitrarily) that replaces of alkyl comprising: for example 2,2-dimethyl-3-(2,2-dimethyl vinyl) cyclopropyl, 3-(2, the 2-dibromo vinyl)-2,2-dimethyl cyclopropyl, 3-(2, the 2-dichloroethylene)-2,2-dimethyl cyclopropyl and 3-(2,2-chloro trifluoro vinyl)-2,2-dimethyl cyclopropyl.
For T 1, arbitrarily by C 1-C 3The C that alkyl replaces 3-C 6Cycloalkyloxy comprises: for example encircle propoxy-, cyclobutoxy group, cyclopentyloxy, cyclohexyloxy and 1-methyl ring propoxy-.
For T 1, the C that is replaced by phenyl 2-C 4(described phenyl is arbitrarily by halogen or C for alkenyl 1-C 4Alkyl replaces) comprising: for example 1-phenyl vinyl, 2-phenyl vinyl, 2-(2-chloro-phenyl-) vinyl, 2-(3-chloro-phenyl-) vinyl, 2-(4-chloro-phenyl-) vinyl, 2-(4-aminomethyl phenyl) vinyl, 2-(2, the 6-difluorophenyl) vinyl, 2-(2, the 5-3,5-dimethylphenyl) vinyl, 1-methyl-2-phenyl vinyl, 2-phenyl-1-propenyl, 2-(4-bromophenyl)-1-propenyl and 2-(2,4, the 6-trimethylphenyl)-the 1-propenyl.
For G, R, T 1, T 2, T 3, R 1, W, X, Y, Y 1, Y 2With Z, alkoxyl group can be to have the straight or branched alkoxyl group of specifying carbonatoms, comprise: methoxyl group for example, oxyethyl group, positive propoxy, isopropoxy, n-butoxy, isobutoxy, sec-butoxy, tert.-butoxy, n-pentyloxy, 1-methyl butoxy, 2-methyl butoxy, 3-methyl butoxy, 1,1-dimethyl propoxy-, 1,2-dimethyl propoxy-, 2,2-dimethyl propoxy-, 1-ethyl propoxy-, positive hexyloxy, 1-methyl pentyloxy, 2-methyl pentyloxy, 3-methyl pentyloxy, 4-methyl pentyloxy, 1,1-dimethyl butoxy, 1,2-dimethyl butoxy, 1,3-dimethyl butoxy, 2,2-dimethyl butoxy, 2,3-dimethyl butoxy, 3,3-dimethyl butoxy, 1-ethyl butoxy, 2-ethyl butoxy, 1,1,2-trimethylammonium propoxy-, 1,2,2-trimethylammonium propoxy-, 1-ethyl-1-methyl propoxy-, 1-ethyl-2-methyl propoxy-, positive heptan the oxygen base, n-octyloxy and n-decyloxy.
For G, R and T 1, C 3-C 6Halogenated cycloalkyl comprises: for example fluoro cyclopropyl, difluoro cyclopropyl, chloro cyclopropyl, dichloro cyclopropyl, 1-methyl-2,2-dichloro cyclopropyl, chloro cyclobutyl, dichloro cyclobutyl, chloro cyclopentyl, dichloro cyclopentyl, chloro cyclohexyl, dichloro cyclohexyl and ptfe ring butyl.
For G, R, R 1, T 1, W, X, Y, Y 1With Z ,-NU 1U 2Comprise: methylamino-for example; ethylamino; the n-propylamine base; isopropylamino; the n-butyl amine base; isobutyl amino; Zhong Ding amino; uncle's fourth amino; the pentylamine base; 1-methyl fourth amino; 2-methyl fourth amino; 3-methyl fourth amino; 1; 1-dimethyl propylene amino; 1; 2-dimethyl propylene amino; 2; 2-dimethyl propylene amino; 1-ethyl third amino; just oneself is amino; 1-methylpent amino; 2-methylpent amino; 3-methylpent amino; 4-methylpent amino; 1; 1-dimethyl butyrate amino; 1; 2-dimethyl butyrate amino; 1; 3-dimethyl butyrate amino; 2; 2-dimethyl butyrate amino; 2; 3-dimethyl butyrate amino; 3; 3-dimethyl butyrate amino; 1-ethyl fourth amino; 2-ethyl fourth amino; 1; 1; 2-trimethylammonium third amino; 1; 2; 2-trimethylammonium third amino; 1-ethyl-1-methyl-prop amino; 1-ethyl-2-methyl-prop amino; dimethylamino; diethylin; two n-propylamine bases; diisopropylaminoethyl; two n-butyl amine bases; di-secondary fourth amino; two isobutyl amino; two pentylamine bases; two is just own amino; the methyl ethylamino; methyl-prop amino; methyl isopropyl amino; methyl fourth amino; methyl Zhong Ding amino; methyl isobutyl amino; methyl-tert fourth amino; methylpent amino; oneself is amino for methyl; ethyl third amino; the ethyl isopropylamino; ethyl fourth amino; ethyl Zhong Ding amino; ethyl isobutyl amino; ethyl penta amino; oneself is amino for ethyl; phenylamino; benzyl amino; N-methyl kharophen; N-ethyl kharophen; N-phenyl kharophen and N-ethanoyl kharophen are wherein used the described substituent appointment carbon atom number range of formation.
For E, G, R, R 1, T 1, W, X, Y, Y 1, Y 2With Z, C 2-C 5Carbalkoxy comprises: for example methoxycarbonyl, ethoxycarbonyl, the positive third oxygen carbonyl, the different third oxygen carbonyl, positive butoxy carbonyl, secondary butoxy carbonyl, isobutyl boc and tertbutyloxycarbonyl.
For G, R, T 1, W, X, Y and Z, C 1-C 4Halogenated alkoxy can be the C of straight or branched 1-C 4Halogenated alkoxy comprises: for example fluorine methoxyl group, difluoro-methoxy, trifluoromethoxy, a chlorine difluoro-methoxy, monobromo difluoro-methoxy, dichloro one fluorine methoxyl group, chlorine methoxyl group, dichloro methoxyl group, trichlorine methoxyl group, bromine methoxyl group, fluorine oxyethyl group, chloroethoxy, bromine oxethyl, difluoroethoxy, trifluoro ethoxy, tetrafluoro oxyethyl group, five fluorine oxyethyl groups, three chloroethoxies, trifluoro one chloroethoxy, fluorine propoxy-, chlorine propoxy-, bromine propoxy-, fluorine butoxy, chlorine butoxy, fluorine isopropoxy and chlorine isopropoxy.
For E, G, R, T 2, T 3, W, X, Y and Z, C 1-C 4Alkylthio comprises: for example methylthio group, ethylmercapto group, positive rosickyite base, iprotiazem base, positive butylthio, isobutyl sulfenyl, secondary butylthio and uncle's butylthio.
For E, G, R, X, W, Y and Z, C 1-C 4Alkyl sulphinyl comprises: for example methylsulfinyl, ethyl sulfinyl, n-propyl sulfinyl, sec.-propyl sulfinyl, normal-butyl sulfinyl, isobutyl-sulfinyl, sec-butyl sulfinyl and tertiary butyl sulfinyl.
For B, E, G, R, W, X, Y and Z, C 1-C 4Alkyl sulphonyl comprises: for example methyl sulphonyl, ethylsulfonyl, n-propyl alkylsulfonyl, sec.-propyl alkylsulfonyl, normal-butyl alkylsulfonyl, isobutyl-alkylsulfonyl, sec-butyl alkylsulfonyl and tertiary butyl alkylsulfonyl.
For B, G, R, R 1, T 1, Y, Y 1And Y 2, C 2-C 4Alkoxyalkyl comprises: C for example 1-C 3Alkoxy methyl, C 1-C 2Alkoxyethyl, methoxy ethoxy methyl and methoxy-propyl.
For E, G, R, R 1, U 1, U 2, Y 1, Y 2With W, C 2-C 4Alkyl-carbonyl comprises: for example ethanoyl, propionyl, butyryl radicals and isobutyryl.
For G and W, C 2-C 6Halogenated alkyl carbonyl comprises: for example chloracetyl, trifluoroacetyl group, 3,3,3-trifluoropropyl acyl group and five fluorine propionyls.
For G, R and Y, C 2-C 5Haloalkyl carbonyl oxygen base comprises: for example chloroethene acyloxy, trifluoroacetyl oxygen base, 3,3,3-trifluoropropyl acyloxy and five fluorine propionyloxies.
For G and Y, C 3-C 7Dialkyl amido carbonyl oxygen base comprises: for example dimethylamino carbonyl oxygen base, diethylin carbonyl oxygen base and diisopropylaminoethyl carbonyl oxygen base.
For R, Y, Z and T 1, naphthyl comprises: for example 1-naphthyl and 2-naphthyl.
For G and T 1, the pyridyl that is replaced by Z comprises arbitrarily: for example 2-pyridyl, 3-pyridyl and 4-pyridyl, and all above-mentioned groups are all replaced by Z arbitrarily; Preferred the two 2-pyridyl and 3-pyridyl that is all replaced by Z arbitrarily; And the more preferably 2-pyridyl that is replaced by Z arbitrarily.
For G and T 1, the pyridyloxy that is replaced by Z comprises arbitrarily: for example 2-pyridyloxy, 3-pyridyloxy and 4-pyridyloxy, and all above-mentioned groups are all replaced by Z arbitrarily.
For R and R 1, the pyridyl that is replaced by X comprises arbitrarily: for example 2-pyridyl, 3-pyridyl and 4-pyridyl, and all above-mentioned groups are all replaced by X arbitrarily; Preferred the two 2-pyridyl and 3-pyridyl that is all replaced by X arbitrarily; And the more preferably 2-pyridyl that is replaced by Z arbitrarily.
For R and R 1, the pyridyloxy that is replaced by X comprises arbitrarily: for example 2-pyridyloxy, 3-pyridyloxy and 4-pyridyloxy, and all above-mentioned groups are all replaced by X arbitrarily.
For R and R 1, the thienyl that is replaced by X comprises arbitrarily: for example 2-thienyl and 3-thienyl, and the two is all replaced by X arbitrarily.
For G and Y 1, the thienyl that is replaced by Z comprises arbitrarily: for example 2-thienyl and 3-thienyl, and the two is all replaced by Z arbitrarily.
For G, R, R 1, Y and Y 1,-N=CT 1T 2Expression alkylidene amino, benzylidene amino, arylidene amino or cycloalkylidene amino comprise: for example methene amido, ethyleneimino, propylidene amino, isopropylidene amino, 4-methyl-2-pentylidene amino, cyclopentylidene amino and cyclohexylidene amino.
For E, C 2-C 4Alkyl amino-carbonyl comprises: for example methylamino carbonyl, ethylamino carbonyl and n-propyl aminocarboxyl.
For E, C 3-C 9Dialkyl amino carbonyl comprises: for example dimethylamino carbonyl, diethylamino carbonyl, di aminocarboxyl, diisopropylaminoethyl carbonyl and di-n-butyl aminocarboxyl.
For B, C 1-C 4Alkyl amino sulfonyl comprises: for example methylamino alkylsulfonyl, ethylamino alkylsulfonyl, n-propyl amino-sulfonyl, sec.-propyl amino-sulfonyl and normal-butyl amino-sulfonyl.
For B, C 2-C 8Dialkyl amino sulfonyl comprises: for example dimethylamino alkylsulfonyl, diethylamino alkylsulfonyl, di amino-sulfonyl, diisopropylaminoethyl alkylsulfonyl and di-n-butyl amino-sulfonyl.
For B, C 2-C 5Thio-alkyl amino-carbonyl comprises: for example amino thiocarbonyl of methylamino thiocarbonyl, ethylamino thiocarbonyl, n-propyl, the amino thiocarbonyl of sec.-propyl and the amino thiocarbonyl of normal-butyl.
For B, C 3-C 9The dialkyl amido thiocarbonyl comprises: for example amino thiocarbonyl of dimethylamino thiocarbonyl, diethylamino thiocarbonyl, di, diisopropylaminoethyl thiocarbonyl and the amino thiocarbonyl of di-n-butyl.
For B, the C that is replaced by benzoyl 1-C 4(described benzoyl is arbitrarily by halogen atom or C for alkyl 1-C 4Alkyl replaces) comprising: for example phenacyl, 2-fluorobenzoyl methyl, 3-chlorobenzoyl methyl, 4-bromobenzene formyl methyl, 2-toluyl methyl, 3-ethylbenzoyl methyl, 4-sec.-propyl phenacyl and 4-tertiary butyl phenacyl.
For B, arbitrarily by halogen atom or C 1-C 4The benzenesulfonyl that alkyl replaces comprises: for example 2-fluorobenzene alkylsulfonyl, 4-fluorobenzene alkylsulfonyl, 2-chlorobenzene alkylsulfonyl, 4-chlorobenzene alkylsulfonyl, 4-bromobenzenesulfonyl, 2; 5-dichlorobenzene alkylsulfonyl, penta fluoro benzene alkylsulfonyl, 4-Methyl benzenesulfonyl base, 2-Methyl benzenesulfonyl base, 4-tert.-butylbenzene alkylsulfonyl, 2; 5-dimethyl benzene alkylsulfonyl, 2; 4-dimethyl benzene alkylsulfonyl, 2; 4; 6-Three methyl Benzene alkylsulfonyl and 2,4,6-tri isopropyl benzenesulfonyl base.
For G and B, C 2-C 5The cyano group alkyl comprises: for example cyano methyl, 2-cyano ethyl, 3-cyano group propyl group and 1-cyano group-1-methylethyl.
For B, C 3-C 9Alkoxycarbonyl alkyl can be a straight or branched, comprising: methoxycarbonyl methyl for example, ethoxycarbonylmethyl group, the positive third oxygen carbonyl methyl, the different third oxygen carbonyl methyl, positive butoxy carbonyl methyl, the isobutyl boc methyl, the tertiary butyloxycarbonyl ylmethyl, just own oxygen carbonyl methyl, positive heptan oxygen carbonyl methyl, 1-methoxycarbonyl ethyl, the 2-ethoxycarbonyl-ethyl, 1-n-butoxy ethyl, 2-methoxycarbonyl ethyl, the 2-ethoxycarbonyl-ethyl, 1-methoxycarbonyl propyl group, 3-ethoxycarbonyl propyl group, 4-methoxycarbonyl butyl, 6-ethoxycarbonyl hexyl, 1-methoxycarbonyl-1-methylethyl, different third oxygen carbonyl of 1--1-methylethyl and 1-ethoxycarbonyl-2-methyl propyl group.
For B, basic metal comprises: for example lithium, sodium and potassium.
For B, alkaline-earth metal comprises: for example magnesium, calcium, strontium and barium, preferably magnesium, calcium and barium.
For B, ammonium NHT 4T 5T 6Comprise: for example ammonium ion, monomethyl ammonium, dimethylammonio, trimethylammonium ammonium, diethyl ammonium, triethyl ammonium, di-isopropyl ammonium, diisopropylethylammoinum base, hexyl methyl ammonium, cyclopropyl methyl ammonium, cyclohexyl methyl ammonium, allyl methyl ammonium, benzyl methyl ammonium and 4-methylcyclohexyl ethyl ammonium; T 4, T 5And T 6In any two can form heterocycle with the nitrogen-atoms of institute's bonding, and described heterocycle is for containing 5,6,7 or 8 yuan of ammoniums of aerobic, nitrogen and/or sulphur atom arbitrarily.
For G, (described phenyl is arbitrarily by halogen or C by methoxyl group that phenyl replaces 1-C 4Alkyl replaces) comprising: for example benzyloxy, 2-chlorine benzyloxy, 3-chlorine benzyloxy, 4-chlorine benzyloxy, 3-methyl benzyloxy, 4-tertiary butyl benzyloxy, 2,6-difluoro benzyloxy and 2-fluoro-4-chlorine benzyloxy.
Containing 5,6,7 or 8 yuan of heterocycle ammoniums of aerobic, nitrogen and/or sulphur atom arbitrarily, is by T 4, T 5And T 6In any two nitrogen-atoms with institute's bonding form, comprising: for example tetramethyleneimine, pyrazolidine, imidazolidine, oxazolidine, isoxazole alkyl, thiazolidine, piperidines, piperazine, morpholine, parathiazan, hexamethylene imine and heptamethylene imines.
For G, R, W, Y and Z, halogenated alkylthio can be the C of straight or branched 1-C 4Halogenated alkylthio comprises: for example fluorine methylthio group, a chlorine difluoro methylthio group, monobromo difluoro methylthio group, trifluoromethylthio, trichloro-methylthio, 2,2,2-trifluoro ethylmercapto group, 1,1,2,2-tetrafluoro ethylmercapto group, fluorine ethylmercapto group, five fluorine ethylmercapto groups and fluorine iprotiazem base.
For G, R, W, Y and Z, the haloalkyl sulfinyl can be the C of straight or branched 1-C 4The haloalkyl sulfinyl; comprise: for example methyl fluoride sulfinyl, a chlorodifluoramethyl-sulfinyl, a bromine difluoro methyl sulfinyl, trifluoromethyl sulphinyl base, trichloromethyl sulfinyl, 2; 2; 2-trifluoroethyl sulfinyl, 1; 1; 2,2-tetrafluoro ethyl sulfinyl, fluoro ethyl sulfinyl, pentafluoroethyl group sulfinyl and fluorine sec.-propyl sulfinyl.
For G, R, W, Y and Z, halogenated alkyl sulfonyl can be the C of straight or branched 1-C 4Halogenated alkyl sulfonyl; comprise: for example methyl fluoride alkylsulfonyl, a chlorodifluoramethyl-alkylsulfonyl, a bromine difluoro methyl alkylsulfonyl, trifluoromethyl sulfonyl, trichloromethyl alkylsulfonyl, 2; 2; 2-trifluoroethyl alkylsulfonyl, 1; 1; 2,2-tetrafluoro ethylsulfonyl, fluoro ethyl alkylsulfonyl, pentafluoroethyl group alkylsulfonyl and fluorine sec.-propyl alkylsulfonyl.
For G, R, T 1With W, halogenated alkenyl can be the C of straight or branched 2-C 4Halogenated alkenyl comprises: for example 2-chlorovinyl, 2-bromo vinyl and 2,2-dichloroethylene.
For G, R, R 1, T 1, W, Y and Y 1, alkenyloxy can be the C of straight or branched 2-C 4Alkenyloxy comprises: for example allyloxy, 2-propenyloxy group, 2-butylene oxygen base and 2-methyl-2-propenyloxy group.
For G, R, W and Y, the halo alkenyloxy can be the C of straight or branched 2-C 4The halo alkenyloxy comprises: 3-chloro-2-propenyloxy group, 3 for example, 3-two chloro-2-propenyloxy groups, 4-chloro-2-butylene oxygen base, 4,4-two chloro-3-butenyloxies and 4,4-two fluoro-3-butenyloxies.
For G, R, W, X, Y and Z, alkenyl thio can be the C of straight or branched 2-C 4Alkenyl thio comprises: allyl sulfenyl, 2-propylene sulfenyl, 2-butylene sulfenyl and 2-methyl-2-propylene sulfenyl for example.
For G, R, W, X, Y and Z, the alkenyl sulfinyl can be the C of straight or branched 2-C 4The alkenyl sulfinyl comprises: allyl group sulfinyl, 2-propenyl sulfinyl, crotyl sulfinyl and 2-methyl-2-propenyl sulfinyl for example.
For G, R, W, X, Y and Z, the alkenyl alkylsulfonyl can be the C of straight or branched 2-C 4The alkenyl alkylsulfonyl comprises: allyl group alkylsulfonyl, 2-propenyl alkylsulfonyl, crotyl alkylsulfonyl and 2-methyl-2-propenyl alkylsulfonyl for example.
For G, R, W and Y, the halo alkenyl thio can be the C of straight or branched 2-C 4The halo alkenyl thio comprises: for example 3-chloro-2-propylene sulfenyl, 4-chloro-2-butylene sulfenyl, 3,3-two chloro-2-propylene sulfenyls, 4,4-two chloro-3-butylene sulfenyls and 4,4-two fluoro-3-butylene sulfenyls.
For G, R, W and Y, the halogenated alkenyl sulfinyl can be the C of straight or branched 2-C 4The halogenated alkenyl sulfinyl comprises: 3-chloro-2-propenyl sulfinyl, 3 for example, 3-two chloro-2-propenyl sulfinyls, 4-chloro-crotyl sulfinyl, 4,4-two chloro-3-butenyl sulfinyls and 4,4-two fluoro-3-butenyl sulfinyls.
For G, R, W and Y, the halogenated alkenyl alkylsulfonyl can be the C of straight or branched 2-C 4The halogenated alkenyl alkylsulfonyl comprises: 3-chloro-2-propenyl alkylsulfonyl, 3 for example, 3-two chloro-2-propenyl alkylsulfonyls, 4-chloro-crotyl alkylsulfonyl, 4,4-two chloro-3-butenyl alkylsulfonyls and 4,4-two fluoro-3-butenyl alkylsulfonyls.
For G, R and W, C 2-C 4The halo alkynyl comprises: for example chloroethene alkynyl, bromoacetylene base, iodoacetylene base, 3-chloro-1-propyne base and 3-bromo-ethyl acetylene base.
For G, R, W and Y, C 2-C 4Alkynyloxy group comprises: for example 2-third alkynyloxy group, 2-butyne oxygen base and 1-methyl-2-third alkynyloxy group.
For G, R, W and Y, C 2-C 4The halo alkynyloxy group comprises: for example 3-chloro-2-third alkynyloxy group, 3-bromo-2-third alkynyloxy group and 3-iodo-2-third alkynyloxy group.
For G, R, W and Y, C 2-C 6The alkynes sulfenyl comprises: 2-propine sulfenyl, 2-butyne sulfenyl and 1-methyl-2-propine sulfenyl for example.
For G, R, W and Y, C 2-C 6Alkynes sulfenyl sulfinyl is drawn together: for example 2-propynyl sulfinyl, 2-butyne base sulfinyl and 1-methyl-2-propynyl sulfinyl.
For G, R, W and Y, C 2-C 6Alkynes sulfenyl alkylsulfonyl is drawn together: for example 2-propynyl alkylsulfonyl, 2-butyne base alkylsulfonyl and 1-methyl-2-propynyl alkylsulfonyl.
For G, R, W and Y, C 2-C 6The acetylenic halide sulfenyl comprises: for example 3-chloro-2-propine sulfenyl, 3-bromo-2-propine sulfenyl and 3-iodo-2-propine sulfenyl.
For G, R, W and Y, C 2-C 6Halo alkynyl sulfinyl comprises: for example 3-chloro-2-propynyl sulfinyl, 3-bromo-2-propynyl sulfinyl and 3-iodo-2-propynyl sulfinyl.
For G, R, W and Y, C 2-C 6Halo alkynyl alkylsulfonyl comprises: for example 3-chloro-2-propynyl alkylsulfonyl, 3-bromo-2-propynyl alkylsulfonyl and 3-iodo-2-propynyl alkylsulfonyl.
For G, R, W and Y, C 2-C 4Alkyl carbonyl oxy comprises: for example acetoxyl group, propionyloxy, butyryl acyloxy and sec.-propyl carbonyl oxygen base.
For E and G; the benzoyl that is replaced by X comprises arbitrarily: for example benzoyl, 2-chlorobenzene formacyl, 3-chlorobenzene formacyl, 4-chlorobenzene formacyl, 4-benzoyl bromide, 4-fluoro benzoyl, 3-methyl benzoyl, 4-methyl benzoyl, 4-tert.-butylbenzene formyl radical and 3,4-dichloro-benzoyl base.
Even when lower concentration, The compounds of this invention also can effectively prevent various insects, and described insect comprises: for example so-called agriculture harmful insect, the crop and the tree of this insect damage agricultural and horticulture; So-called domestic animal harmful insect, this insect lives on one's body the livestock and poultry; So-called health harmful insect, this insect produces various negative impacts to the environment (comprising the house) that the mankind lived; So-called stock harmful insect, the cereal of storing in this insect damage warehouse; And live in above-mentioned same position and to the above-mentioned prejudicial mite of content, nematode, mollusk and the crustaceans etc. mentioned.
The harmful insect of being eliminated of the following stated, mite, nematode, mollusk and crustacean example by The compounds of this invention, still, the example that is not limited only to be exemplified out.
The lepidopteran harmful insect, for example striped rice borer ( Chilo suppressalisWalker), Cnaphalocrocis medinali(rice leaf roller) ( Cnaphalocrocis medinalisQuen é e), rice green caterpillar ( Naranga aenescensMoore), rice plant skipper ( Naranga guttataBremer et Gvey), small cabbage moth ( Plutella xylostellaLinn é), the wild cabbage casemaking clothes moth ( Mamestra brassicaeLinn é), the dish miller ( Pieris rapae crucivoraBoisduval), the turnip casemaking clothes moth ( Agrotis segetumDenis et Schifferm ü ller), the twill casemaking clothes moth ( Spodptera lituraFabricius), beet armyworm ( Spodoptera exiguaH ü bner), rouleau (leaf) moth ( Adoxophyes sp.), tea long paper moth ( Homona magnanimaDiakonoff), peach fruit moth ( Carposina NiponensisWalsingham), oriental fruit months ( Grapholita molestaBusck), adoxophyes moth ( Adoxophyes orana fasciataWalsinghm), apple leaf miner ( Phyllonorycter ringoniellaMatsumura), corn earworm ( Helicoverpa zeaBoddie), Heliothis virescens ( Heliothis virescensFabricius), Pyrausta nubilalis (Hubern). ( Ostrinia NubilalisH ü bner), the meadow covet noctuid ( Spodoptera frugiperdaJ.E. Smith), the moth-eaten moth of apple ( Cydia pomonellaLinn é), fall webworms ( Hyphantria cuneaDrury) etc.;
The Hemiptera harmful insect, for example rice green leafhopper ( Nephotettix cincticepsUhler), Nilaparvata lugen (brown planthopper) ( Nilaparvata lugensStal), black peach aphid ( Myzus persicaeSulzer), cotten aphid ( Aphis gossypiiGlover), trialeurodes vaporariorum ( Trialeurodes vaporariorumWestwood), sweet potato whitefly ( Bemisia tabaciGennadius), pear psyllid ( Psylla PyricolaF_rster), intend pear lace bug ( Stephanitis pyrioidesScott), arrowhead scales ( Unaspis yanonensisKuwana), the Kang Shi mealybug ( Pseudococcus comstockiKuwana), ceroplastes rubens ( Ceroplastes rubensMaskell), brown rock line stinkbug (brown-marmorated stinkbug) ( Halyomorpha mistaUhler), the wild cabbage cabbage bug ( Eurydema rugosamMotschulsky), bedbug ( Cimex lectulariusLinn é);
The Coleoptera harmful insect, for example ladybug of eggplant 28 stars ( Henosepilachna VigintioctopunctataFabricius), big green rutelian first ( Anomala cupreaHope), american rice weevil ( Lissorhoptrus oryzophilusKuschel), cylas formicarius ( Cylas formicariusFabricius), aulacophora femoralis ( Aulacophora femoralisMotschulsky), cabbage flea beetle ( Phyllotreta striolataFablicius), hickie wax longicorn ( Anoplophora malasiacaThomson), ponderous borer ( Monochamus alternatusHope), bar chrysomelid ( Diabrotica spp.), sitophilus zea-mais ( Sitophilus zeamaisMotschulsky), rice weevil ( Sitophilus oryzaeLinn é), grain weevil ( Sitophilus GranariusLinn é), red flour beetle ( Tribolium castaneumHerbst) etc.;
The Diptera harmful insect, for example Americal rice leaf miner ( Liriomyza trifoliiBurgess), plant fly ( Delia platuraMeigen), hessian fly ( Mayetiola destructorSay), the melon trypetid ( Dacus (Zengodacus) cucurbitaeCoquillett), Mediterranean fruitfly ( Ceratitis CapitataWiedemann), housefly ( Musca domesticaLinn é), tatukira ( Stomoxys calcitransLinn é), sheepked ( Melophagus orinus), heel fly ( Hypoderm lineatumDevillers), bomb fly ( Hypoderma borisLinn é), sheep nose fly ( Oestrus ovisLinn é), tsetse fly ( GolossinaPalpalis Robineau-Desvoidy), culex pipiens pollens ( Culex pipiens pallensCoquillett), Aedes aegypti ( Aedes aegyptiLinn é), Anopheles culicifacies Anopheles culicifacies) etc.;
The Hymenoptera harmful insect, for example cabbage sawfly ( Athalis rosae ruficornisJakovlev), neodiprion sertifer ( Neodiprion sertiferGeoffroy), chestnut oak sawfly chestnutsawfly ( Apethymus kuriTakeuchi) etc.;
The Thysanoptera harmful insect, for example pale brown thrips ( Thrips palmiKarny), cotton thrips ( Thrips tabaciLindeman), alfalfa thrips ( Frankliniella occidentalisPergande), flower thrips ( Frankliniella intonsaTrybom), tea golden thistle horse ( Scirtothrips dorsalisHood) etc.;
The Dictyoptera harmful insect, for example smoke Perilpaneta americana ( Periplaneta fuliginosaServille), Japanese blattaria ( Periplaneta japonicaKarny), Groton bug ( Blattella germanicaLinn é) etc.;
The Orthoptera harmful insect, for example the Asia migratory locusts ( Locusta migratoriaLinn é), Hokkaido oryza chinensis ( Oxya yezoensisShiraki), desert locust ( Schistocerca gregariaForsk_l) etc.;
The Isoptera harmful insect, for example Coptotermes formosanus Shtrari ( Coptotermes formosanusShiraki), ( Reticulitermes (Leucotermes) speratusKolbe), blackwing subterranean ( Odontotermes formosanusShirakif) etc.;
The Siphonaptera harmful insect, for example cat comb head disturb ( Ctenocephalides felisBouch é), Pulex irritans ( Pulex irritansLinn é), the east mouse disturb ( Xenopsylla cheopisRothschild) etc.;
The Mallophaga harmful insect, for example the chick poultry louse ( Menacanthus stramineusNitsch), the ox poultry louse ( Bovicola bovisLinn é);
The Anoplura harmful insect, for example wealthy chest blood lice ( Haematopinus eurysternusNitzsh), haematopinus suis ( Haematopinus suisLinn é), Linognathus vituli ( Linognathus vituliLinn é), side pipe pipe lice ( Solenopotes capillatusEnderlein) etc.;
Section pest mite, for example oranges and tangerines pawl mite ( Panonychus citriMcGregor), panonychus ulmi ( Panonychus ulmiKock), T.urticae Koch ( Tetranychus urticaeKoch), kamisawa tetranychus ( Tetranychus kanzawaiKishida) etc.;
The Eriophyidae insect, for example pink citrus rust mite ( Aculops pelekassiKeifor), pears leaf rust mite ( Epitrimerus pyriNalepa), turmeric goitre mite ( Aceria TulipaeKeiter), pink tea rust mite ( Acaphylla theaeWatt) etc.;
The Tarsonemidae insect, for example Polyphagotarsonemus latus Banks ( Polyphagotarsonemus latusBanks), the narrow tarsonemid mite of primrose ( Steneotarsonemus pallidusBanks) etc.;
The Tyroglyphidae insect, for example tyrophagus putrescentiae ( Tyrophagus putrescetiaeSchrank), Luo Shi root mite ( Rhizoglyphus robiniClaparede) etc.;
Watt VARROIDAE of mite section insect, for example varoa mite ( Varroa jacobsoniOudemans) etc.;
Hard tick section insect, for example boophilus microplus ( Boophilus microplusCanestrini), haemaphysalis longicornis ( Haemaphysalis longicormnisNeumann) etc.;
The Sarcoptidae insect, for example itch mite ( Sarcaptes scabieiLinn é) etc.;
Nematode, for example Meloidogyne incognita ( Meloidogyne incognitaKofoid etWhite), northern root knot nematode ( Meloidogyne haplaChitwood), Cobb root ( Pratylenchus penetrausCobb), wounded or disabled Pratylenchidae ( Pratylenchus vulnusAllen et Jensen), globodera rostochiensis ( Globodera rostochiensisWollenweber), pine wood nematode ( Bursaphelenchus xylophilusSteiner etBuhrer) etc.;
Mollusk, for example apple snail ( Pomacea canaliculataLamarck), ( Incilaria pilineataBenson), ( Acusta despecta sieboldianaPfeiffer), ( Euhadra peliomphalaPfeiffer), pillworm ( Armadillidium vulgareLatreille) etc.;
Crustachia, for example pillworm ( Armadillidium vulgareLatreille) etc.
The crop pest of being controlled by The compounds of this invention is as follows:
Rice blast ( Pyricularia oryzae), Helminthosporium of brown spot of rice ( Cochliobolus Miyabeanus) and the sheath and culm blight of rice ( Rhizoctonia solani);
Powdery mildew of cereals ( Erysiphe graminis f.sp.hordei, f.sp.tritici), stripe disease of barley ( Pyrenophora graminea), net blotch of barley ( Pyrenophora teres), Gibberella zeae (Sch.) Petch ( Gibberella zeae), stripe or yellow rust of cereals ( Puccina striiformis, P.graminis, P.reconditaWith P.hordei), snow blight and snow mould ( Typhula sp., Micronectriella Nivais), loose smut of wheat ( Ustilage tritici, U.nuda), eye spot ( Pseudocercorsporella herpotrichoides), barley leaf blotch ( Rhynchosporium Secalis), wheat dead leaf disease ( Septoria tritici), wheat glume blight ( Leptosphaeria Nodorum);
Oranges and tangerines resin disease ( Diaporthe citri), the oranges and tangerines pinta ( Elsinoe fawcetti), and citrus common green mold ( Penicillium digitatum, P.italicum);
The apple flower mildew ( Sclerotinia mali), the mildew and rot disease of apple ( Valsa mali), apple mildew ( Podosphaera leucotricha), the apple zonate spot ( Alternaria mali) and scab of apple ( Venturia inaequalis);
Pear scab ( Venturia nashicola), the pears black spot ( Alternaria Kikuchiana) and rust of pear ( Gymnosporangium haraeanum);
Peach brown rot ( Sclerotinia cinerea), the peach pinta ( Cladosporium Carpophilum) and the rotten disease of peach Phomopsis Phomopsis rot (Phomopsis sp.);
Downy mildew of garpe ( Plasmopara viticola), grapevine anthracnose ( Elsinoe Ampelina), bitter rot or anthracnose of grape ( Glomerlla cingulata), uncinula necator ( Uncinula Necator) and the grape rust ( Phakopsora ampelopsidis);
Anthracnose of kaki ( Gloesporium kaki), persimmon Powdery Mildew (Phyllactinia kakicola), persimmon angular leaf spot ( Cercospora kaki), leaf spot of kaki ( Mycosphaerella nawae);
The pumpkin cream mildew ( Pseudoperenospora cubensis), pumpkin anthrax ( Colletotrichum lagenarium), squash marble dust ( Sphaerotheca fuliginea), the climing rot of pumpkin ( Mycosphaerella melonis);
Tomato late blight ( Phytophthora infestans), early blight of tomato ( Alternaria Solani) and leaf muld of tomato ( Cladosporium fulvam);
Eggplant phomopsis rot ( Phomopsis vexans) and the eggplant Powdery Mildew ( Erysiphe Cichoracoarum);
The brassicaceous vegetable black spot ( Alternaria japonica) and the brassicaceous vegetable leukodermia ( Cerocosporella brassicae);
Big rust of onion ( Puccinia allii);
Purple spot of soybean ( Cercospora kikuchii), the soybean anthrachose of grape ( Elsinoe glycines) and the soybean diplostomiasis ( Diaporthe phaseololum);
Bean anthracnose ( Collectorichum lindemuthianum);
The cercospora black spot of peanut ( Mycosphaerella personatum) and the cercospora brown spot of peanut ( Cercospora arachidicola);
Powdery mildew of pea ( Erysiphe pisi);
Target ( Alternaria solani);
Powdery mildew of strawberry ( Sphaerotheca humuli);
Tea net cake disease ( Exobasidium reticulatum) and the tea leukodermia ( Elsinoe Leucospila);
Alternaria alternate ( Alternaria longipes), the tobacco Powdery Mildew ( Erysiphe Cichoracearum) and Colletotricum destructivum ( Colletotrichum tabacum);
Beet cercospora leaf spot ( Cercospora beticola);
The rose black spot ( Diplocarpon rosae) and rose mildew ( Sphaerotheca Pannosa);
The chrysanthemum leaf spot ( Septoria chrysanthemiindici) and the chrysanthemum rust ( Puccinia Horiana);
The gray mold of various crops ( Botrytis cinerea); And
The sclerotium disease of various crops ( Sclerotinia sclerotiorum).
In addition, even under very low concentration, The compounds of this invention also can prevent hydrobiological adhering to effectively.Hydrobiont of the present invention is meant, for example, shellfish and marine alga, as mussel, barnacle, oyster, hydra (hydrozoan), hydra (hydra), imperial cyprid, Ascidian, red-violet colour marine alga (seamoss), Bagula, mire spiral shell, sea lettuce, green laver, water cloud etc.
Particularly, even when using with lower concentration, The compounds of this invention also can effectively be eliminated various insects and phytopathogen microorganism, as Orthoptera, Hemiptera, lepidopteran, Coleoptera, Hymenoptera, Diptera, Temitidae and mite and lice.In addition, The compounds of this invention prevents effectively that also the various hydrobionts that live in seawater and the fresh water are first-class attached to facility in the water.On the other hand, contain the useful compound that almost Mammals, fish, shellfish and useful insect is not had negative impact in the The compounds of this invention.
E is that the The compounds of this invention of CN can prepare (flow process 1) in accordance with the following methods.
Flow process 1:
(method A)
(method B)
(method C)
Figure C9719404100703
In (flow process 1), Q, A have the implication identical with above-mentioned definition with B; The leavings group that the L representative is suitable is as chlorine atom, bromine atoms, iodine atom, alkoxyl group, phenoxy group with 1 to 4 carbon atom, the alkylsulfonyloxy with 1 to 4 carbon atom, phenylsulfonyloxy, tosyloxy, phenoxy group, 1-pyrazolyl or 1-imidazolyl; L ' represents halogen atom; And the alkyl representative preferably has the alkyl of 1 to 4 carbon atom.
Method A in (flow process 1) is with the acyl chlorides of the acetonitrile derivative of formula (3) and formula (4), ester or acid amides reaction, or obtains The compounds of this invention (1 ') with the anhydride reaction of formula (5).Optional alkylogen with compound (1 ') and formula (8), alkyl sulfonate esters, trimethyl silyl halogenide, SULPHURYL CHLORIDE, sulphonamide chlorine, thiocarbamoyl chlorine, acyl chlorides or ester reaction are to be translated into The compounds of this invention (1).According to the type of B in the The compounds of this invention (1), compound (1 ') and dihydropyrane, isocyanic ester or the reaction of isothiocyanic acid ester are made compound (1).In method A,, under the situation of separating compound (1 ') not, can directly make compound (1) if with excessive use formula (4) or (5) compound.
When Q by nitrogen atom bonding when vinyl cyanide is partly gone up, compound (1 ') can prepare according to method B.Method B is with formula (6) heterogeneous ring compound and the reaction of formula (7) halo cyano group ketone derivatives, makes The compounds of this invention (1 ').
When A by nitrogen atom bonding when vinyl cyanide is partly gone up, compound (1 ') can prepare according to method C.Method C makes The compounds of this invention (1 ') with formula (9) cyanoacetic acid derivative and the reaction of formula (10) heterogeneous ring compound.As the case may be, in the presence of alkali that formula (3) acetonitrile derivative is for example used in method A, will make formula (9) compound with carbonate reaction.
The The compounds of this invention that E is can prepare (flow process 2) in accordance with the following methods.
Flow process 2:
(method D)
Figure C9719404100711
(method E)
Figure C9719404100712
(method F)
Figure C9719404100721
In (flow process 2), the implication of Q, A, E, B, L, L ' and alkyl is the same.
Method D in (flow process 2) is with formula (11) compound and formula (4) acyl chlorides, ester or acid amides reaction, or obtains The compounds of this invention (1 ') with formula (5) anhydride reaction.Choose wantonly compound (1 ') and formula (8) alkylogen, alkyl sulfonate esters, trimethyl silyl halogenide, SULPHURYL CHLORIDE, sulphonamide chlorine, thiocarbamoyl chlorine, acyl chlorides or ester are reacted to be translated into The compounds of this invention (1).According to the type of B in the The compounds of this invention (1), compound (1 ') and dihydropyrane, isocyanic ester or the reaction of isothiocyanic acid ester are made compound (1).In method A,, under the situation of separating compound (1 ') not, can directly make compound (1) if with excessive use formula (4) or (5).
When Q by nitrogen atom bonding to ethylene moiety the time, compound (1 ') can prepare according to method E.Method E reacts formula (6) heterogeneous ring compound and formula (12) compound in the presence of alkali, make The compounds of this invention (1 ').
When A by nitrogen atom bonding to ethylene moiety the time, compound (1 ') can prepare according to method F.Method F makes The compounds of this invention (1 ') with formula (13) compound and the reaction of formula (10) heterogeneous ring compound by dealcoholization.As the case may be, in the presence of alkali that formula (11) acetonitrile derivative is for example used in method D, will make formula (13) compound with carbonate reaction.
In case of necessity, E be the compound (1 ') of carbalkoxy can hydrolysis, decarboxylation and halogenation make the The compounds of this invention that E is a halogen atom.As the case may be, E be halogen atom The compounds of this invention can with make different The compounds of this invention corresponding to the reaction of the nucleophilic reagent (as tris phosphite, alkanethiol, thiophenol, metallic acetylide, metal cyanides, metal azide, nitrite) of E.What can depend on the circumstances equally is that under alkaline condition, E is that the compound (1 ') of carbalkoxy can make The compounds of this invention with the electrophilic reagent reaction by the prepared compound of decarboxylation.
As the case may be, preferably reaction in the presence of alkali of the method for (flow process 1) and (flow process 2).Used alkali comprises: for example, alkali metal alcoholate is as sodium ethylate, sodium methylate and potassium tert.-butoxide; Alkali metal hydroxide is as sodium hydroxide and potassium hydroxide; Alkaline carbonate is as yellow soda ash and salt of wormwood; Organic bases is as triethylamine, pyridine and DBU; Organolithium compound is as butyllithium; Lithium amide is as diisopropylaminoethyl lithium and two trimethyl silyl lithium amide; And sodium hydride.
The reaction of (flow process 1) and (flow process 2) can be carried out in to the solvent of reactionlessness.Described solvent comprises: for example, lower alcohol is as methyl alcohol and ethanol; Aromatic hydrocarbons is as benzene and toluene; Ether is as ether, tetrahydrofuran (THF), 1,4-diox, 1,2-glycol dimethyl ether and 1,2-diethoxyethane; Halohydrocarbon is as methylene dichloride, chloroform and 1,2-ethylene dichloride; Acid amides is as dimethyl formamide and N,N-DIMETHYLACETAMIDE; Acetonitrile; Dimethyl sulfoxide (DMSO); And the mixed solvent of above-mentioned solvent.According to circumstances also can use the mixed solvent that contains above-mentioned solvent and water.What can depend on the circumstances equally is in order to obtain the sound response result, quaternary ammonium salt (as bromination four positive fourth ammoniums) can be added reaction system as catalyzer.Temperature of reaction can freely be set between-30 ℃ and 200 ℃; Preferably, temperature of reaction is reduced between 0 ℃ and 150 ℃, or between 0 ℃ and solvent boiling point, if use solvent.The operable alkali number of reaction substrate is 0.05 to 10 equivalent, preferred 0.05 to 3 equivalent.
According to any ordinary method, The compounds of this invention can be separated from reaction mixture; And if The compounds of this invention needs purifying, the separation of this compound and purifying can be finished by the method for any routine, and described method is recrystallization or column chromatography for example.
Those The compounds of this invention with unsymmetrical carbon comprise (+) type and (-) type optically active compound.
The method of preparation (flow process 1) compound used therefor (3) is as described below.Compound (3) can prepare according to following (flow process 3).
Flow process 3:
1) reaction of the benzyl halide of formula (14), alkylsulphonic acid benzyl ester aryl sulfonic acid benzyl ester, halogenated methyl-heterogeneous ring compound, alkylsulfonyloxy group ylmethyl-heterogeneous ring compound or aryl-sulfonyl oxygen ylmethyl-heterogeneous ring compound and suitable cyanating reagent makes compound (3); Perhaps, phenylacetic acid derivatives or heterocycle acetogenin are converted into the corresponding amide derivative, dehydration makes compound (3) then.
2) in the presence of alkali, heterocyclic halides (15) and cyan-acetic ester (16) condensation are made compound (17); Then, hydrolysis and decarboxylation make compound (3).
3),, Hete rocyclic derivatives (6) (wherein nitrogen-atoms is undersaturated among the Q) and halo acetonitrile derivative are reacted in the presence of alkali to ethylene moiety the time by nitrogen atom bonding as the Q in the compound (3) in order to make this compound; Perhaps, in the presence of alkali, compound (6) and compound (18) reaction are made compound (17), wherein said compound (18) is by making the cyan-acetic ester halogenation; Subsequently, again compound (17) hydrolysis and decarboxylation are made compound (3).
(flow process 2) compound used therefor (11) can make by the mode identical with the preparation of above-claimed cpd (3).
In the presence of alkali,, then the condenses halogenation that generates can be made (flow process 1) used compound (7) by with benzoyl halogen or heterocyclic carboxylic acid carboxylic acid halides and cyanoacetic acid ester condensation.
(described ordinary method is referring to Alan R.Katritzky and Charles W.Rees can to obtain above-mentioned halogenated methyl-heterogeneous ring compound, alkylsulfonyloxy group ylmethyl-heterogeneous ring compound and aryl-sulfonyl oxygen ylmethyl-heterogeneous ring compound from the heterocycle methane Derivatives that makes according to ordinary method or heterocyclic carboxylic acid ester derivative; Comprehensive heterocyclic chemistry (Comprehensive HeterocyclicChemistry), the 2nd volume, the 3rd volume, the 4th volume, the 5th volume or the 6th volume).Q is the compound (14) of oxazole-4-base or thiazole-4-base in order to make wherein, can be with carboxylic acid amide or thioamides and 1, and the reaction of 3-two chloro-2-acetone.
The example of The compounds of this invention is shown in table 1 hereinafter to table 14.The implication of abridging in the table is as follows:
Me: methyl, Et: ethyl, Pr: propyl group, Bu: butyl, Pen: amyl group, Hex: hexyl, Hep: heptyl, Oct: octyl group, Non: nonyl, Dec: decyl, Ph: phenyl, n: just, and i: different, sec: the second month in a season, t: uncle, c: ring.
Figure C9719404100781
B3：CH 3OCH 2-
B4：CF 3SO 2- B5：CH 3SO 2-
Figure C9719404100793
Figure C9719404100794
Figure C9719404100795
Figure C9719404100796
B13：Me 3Si-
Figure C9719404100798
Figure C9719404100799
Figure C9719404100801
B24：CH 3O(CH 2) 2OCH 2-
B26：PhSO 2-
Figure C9719404100803
Figure C9719404100804
B32：CH 3SCH 2- B33：CH 3CH 2OCH 2-
Figure C9719404100805
Figure C9719404100811
Table 1
Figure C9719404100831
R 1 R 2 R 3 B Y 1 Y 2 Y 3
2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph H H H H H H H H H H H H H H H H Cl H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H Me Me Me Me Me Me Me Me Et Et nPr iPr iPr nBu H Cl Me OMe SMe OCF 3 CF 3 CO 2Me H H H H Me Me Cl Cl Cl Me H Me Me Cl Me H H H H H H H H Me Me CF 3 H Me H Me H Me Me H Me Me Me Me
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph H H H H H H Me Cl NO 2 CO 2Me CO 2Et H Me H H Cl Cl Cl Ph H CF 3 H cPr H H H H H H H H H H H H H Me Cl H Cl Cl H Ph H CF 3 H H H H H H H H H H H H H H H H H H B1 H H H H H tBu Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me Me H H H H H H H H Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me H Me CF 3 H H H H H H Me Me Me Me Me Me Me Me Me Me Me Me
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph H OMe H NH 2 H NHMe H NMe 2 H NO 2 H CN H OH H CO 2Me H CO 2Et H H H H H cPr H OMe H NH 2 H NHMe H NMe 2 H NO 2 H CN H OH H CO 2Me H H H H H H H H H H H H H H H H H H H H H H H H H H H H H Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me H CF 3 CF 2H CH 2OMe COMe
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H Cl Cl Cl Br Me Me Br OMe Me OMe H Cl OCF 3 OCF 3 OCF 3 Me Cl SMe Me Cl SMe SOMe Cl Cl Cl CF 3 Me Br Br H Me OMe H OMe OMe Me Cl H OCF 3 OCF 3 Cl SMe SMe H Cl SOMe Ph CH 2Ph Me Me Me H H Me Me H H Me Me Me H Me Me Me Me Me H Me Me
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph H H H H H H H Me Cl Br CF 3 NO 2 CN CO 2Me CO 2Et H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H SOMe SO 2Me Cl SO 2Me CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 H Cl SO 2Me H Me Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl C1 Cl H H Br SMe H Me Me H Me H Me Me Me Me Me Me Me Me Me CF 3 CF 2H CH 2OMe COCH 3 Me H Me Me
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 NO 2 NO 2 NO 2 NO 2 Cl CN CN SOMe SO 2Me CF 3 NO 2 CN NHMe NMe 2 Ph CH 2Ph OPh OH CO 2Me OMe OCF 3 OCF 2H OCF 2H CF 3 Cl Me H NO 2 CF 3 Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me CF 2H Me Me Me H Me Me Me
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H CN CN Cl Br NHMe NHMe NHMe Cl NMe 2 NMe 2 NMe 2 Cl Ph Ph Cl CH 2Ph CH 2Ph Cl OPh OPh Cl OH OH Me H CN CN Me Cl H NHMe Me Cl H NMe 2 Cl H Ph Me H CH 2Ph Cl H OPh Me H Me H Me Me Me Me H Me Me Me H Me Me H Me Me H Me Me H Me Me H
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph H H H H H H H Cl H H H Cl Cl NO 2 CO 2Me CO 2Et H Cl H Cl NO 2 CO 2Me CO 2Et H H H H H H H H H H H H Me H H H H H H H H H H H H H H H H B1 B1 B2 B3 B4 B4 B4 B4 B4 B4 B5 B5 B6 B6 B6 B6 B6 Cl CO 2Me CO 2Me CO 2Me cPr cPr Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl OH Me Cl H Me Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me Me H Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph H Cl NO 2 CO 2Me CO 2Et H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B7 B7 B7 B7 B7 B8 B9 B10 B11 B12 B13 B14 B15 B16 B17 B18 B19 B20 B21 B22 B23 B24 B25 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph H H H H H H H H H H H H H H H Me Cl NO 2 CO 2Me CO 2Et H Cl H H H H H H H H H H H H H H H H H H H H H H H H B26 B27 B28 B29 B30 B31 B32 B33 B34 Na K B1 B2 B3 B4 B4 B4 B4 B4 B4 B5 B5 B6 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph Me Cl NO 2 CO 2Me CO 2Et H Me Cl NO 2 CO 2Me CO 2Et H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B6 B6 B6 B6 B6 B7 B7 B7 B7 B7 B7 B8 B9 B10 B11 B12 B13 B14 B15 B16 B17 B18 B19 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph H H H H H H H H H H H H H H H H H H H H H Me Cl H H H H H H H H H H H H H H H H H H H H H H H B20 B21 B22 B23 B24 B25 B26 B27 B28 B29 B30 B31 B32 B33 B34 Na K B1 B2 B3 B4 B4 B4 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl H H H H H H Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me H H H H H H
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph NO 2 CO 2Me CO 2Et H H NO 2 H Me Cl NO 2 CO 2Me CO 2Et H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B4 B4 B4 B5 B6 B6 B7 B7 B7 B7 B7 B7 B8 B9 B10 B11 B12 B13 B14 B15 B16 B17 B18 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph tBu tBu tBu tBu tBu H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B19 B20 B21 B22 B23 B24 B25 B26 B27 B28 B29 B30 B31 B32 B33 B34 Na K H H H B7 H Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl H Me Me Me Me H H H H H H H H H H H H H H H H H H H H H H Me H H H H H H H H H H H H H H H H H H Me Me CF 3 H Me
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu H Cl H H H H H H H Me Cl NO 2 CO 2Me CO 2Et H Me Cl CF 3 cPr OMe NO 2 CN CO 2Me H H H H H H H H H H H H H H H H H H H H H H H H H H B8 H H H H H B7 B7 B7 B7 B7 H H H H H H H H H Me Me Et Et Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me H Me Me H H H H H H H H Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me Me H Me H Me CF 3 H H H H H H Me Me Me Me Me Me Me Me Me
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu CO 2Et H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B34 H H H H H H H H H H H H Cl Cl Cl Cl Cl Cl Cl Br Me Me Br OMe Me OMe Cl OCF 3 OCF 3 OCF 3 Me Cl SMe Me Cl Cl Cl Cl Cl Cl Cl CF 3 Me Br Br H Me OMe H OMe Me Cl H OCF 3 OCF 3 Cl SMe SMe Me H CF 3 CF 2H CH 2OMe COMe Me Me Me H H Me Me H Me Me Me H Me Me Me Me Me
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu H H H H Me Cl Br CF 3 NO 2 CN CO 2Me CO 2Et H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B7 H H H H H H H H H H H H H H H H H H H H H H SMe CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 H Me Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl H H Br SMe SOMe SO 2Me CF 3 H Me H Me Me Me Me Me Me Me Me Me CF 3 CF 2H CH 2OMe COCH 3 Me H Me Me Me Me Me
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 NO 2 NO 2 NO 2 Cl CN CN CN Cl NMe 2 Cl OH OH Cl NO 2 CN NHMe NMe 2 OH CO 2Me OMe OCF 3 OCF 2H OCF 2H Cl Me H NO 2 Cl Me H CN H NMe 2 Me H OH Me Me Me Me Me Me Me Me Me CF 2H Me Me H Me Me Me H Me H Me Me H Me
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu H H H H Cl H H H Me Cl NO 2 CO 2Me CO 2Et H H Cl H Me Cl NO 2 CO 2Me CO 2Et H H H H H H H H H H H H H H H H H H H H H H H H H H H B1 B1 B2 B3 B4 B4 B4 B4 B4 B4 B5 B6 B6 B7 B7 B7 B7 B7 B7 B8 CO 2Me CO 2Me CO 2Me Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Cl H Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me H Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B9 B10 B11 B12 B13 B14 B15 B16 B17 B18 B19 B20 B21 B22 B23 B24 B25 B26 B27 B28 B29 B30 B31 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu H H H H H H H H H Me Cl NO 2 CO 2Me CO 2Et H H Cl H Me Cl NO 2 CO 2Me CO 2Et H H H H H H H H H H H H H H H H H H H H H H H B32 B33 B34 Na K B1 B2 B3 B4 B4 B4 B4 B4 B4 B5 B6 B6 B7 B7 B7 B7 B7 B7 Cl Cl Cl Cl Cl CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B8 B9 B10 B11 B12 B13 B14 B15 B16 B17 B18 B19 B20 B21 B22 B23 B24 B25 B26 B27 B28 B29 B30 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B31 B32 B33 B34 Na K B1 B2 B3 B4 B5 B6 B7 B8 B9 B10 B11 B12 B13 B14 B15 B16 B17 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl H H H H H H H H H H H H H H H H H Me Me Me Me Me Me H H H H H H H H H H H H H H H H H
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
TBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B18 B19 B20 B21 B22 B23 B24 B25 B26 B27 B28 B29 B30 B31 B32 B33 B34 Na K H H H B7 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl H Me Me Me H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H Me Me CF 3 H
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals H H Cl H H H H H H H Me Cl CF 3 cPr OMe NO 2 CN CO 2Me CO 2Et H Me Cl CF 3 H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 H H H H Me Me Me Et Et Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Cl Cl Me H Me Me H H H H H H H H H H H H Cl Cl Cl Cl Me Me Me Me H Me H Me CF 3 H H H H H H H H H H Me Me Me Me
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals cPr OMe NO 2 CN CO 2Me CO 2Et H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B7 H H H B7 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Br Me Me Br OMe Me OMe Cl OCF 3 OCF 3 OCF 3 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl CF 3 Me Br Br H Me OMe H OMe Me Cl H Me Me Me Me Me Me H CF 3 CF 2H CH 2OMe COMe Me Me Me H H Me Me H Me Me Me H
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals H H H H H H H H H Me Cl Br CF 3 NO 2 CN CO 2Me CO 2Et H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B7 H H H H H H H H H H H H H H H H H Me Cl SMe Me Cl SMe CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 OCF 3 OCF 3 Cl SMe SMe H Me Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl H H Me Me Me Me Me H Me H Me Me Me Me Me Me Me Me Me CF 3 CF 2H CH 2OMe COCH 3 Me H
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B7 H H H H H CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 NO 2 NO 2 NO 2 Cl CN CN CN Cl Br SMe SOMe SO 2Me CF 3 NO 2 CN NHMe NMe 2 OH CO 2Me OMe OCF 3 OCF 2H OCF 2H Cl Me H NO 2 Cl Me H CN Me Me Me Me Me Me Me Me Me Me Me Me Me Me CF 2H Me Me H Me Me Me H Me
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals H H H H H H H H H H H H H H H Cl H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B1 B2 B3 B4 B5 B6 B7 B7 B8 B9 B10 B11 B12 B13 B14 NMe 2 Cl OH OH Cl CO 2Me CO 2Me CO 2Me Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl H NMe 2 Me H OH Me Cl H Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl H Me Me H Me Me Me H Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B15 B16 B17 B18 B19 B20 B21 B22 B23 B24 B25 B26 B27 B28 B29 B30 B31 B32 B33 B34 Na K B1 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl CF 3 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals H H H Cl CO 2Me H H H Cl NO 2 CO 2Me H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B2 B3 B4 B4 B4 B5 B6 B7 B7 B7 B7 B8 B9 B10 B11 B12 B13 B14 B15 B16 B17 B18 B19 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals H H H H H H H H H H H H H H H H H H H H H Me Cl H H H H H H H H H H H H H H H H H H H H H H H B20 B21 B22 B23 B24 B25 B26 B27 B28 B29 B30 B31 B32 B33 B34 Na K B1 B2 B3 B4 B4 B4 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl H H H H H H Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me H H H H H H
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals NO 2 CO 2Me CO 2Et H H NO 2 H Me Cl NO 2 CO 2Me CO 2Et H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B4 B4 B4 B5 B6 B6 B7 B7 B7 B7 B7 B7 B8 B9 B10 B11 B12 B13 B14 B15 B16 B17 B18 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 3-pyridine radicals 3-pyridine radicals 3-pyridine radicals 3-pyridine radicals 3-pyridine radicals H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B19 B20 B21 B22 B23 B24 B25 B26 B27 B28 B29 B30 B31 B32 B33 B34 Na K H H H B4 B7 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl CF 3 Cl Cl Cl H H H H H H H H H H H H H H H H H H Cl Cl H H H H H H H H H H H H H H H H H H H H H Me Me H H H
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
4-pyridine radicals 4-pyridine radicals 4-pyridine radicals 4-pyridine radicals 4-pyridine radicals 3-Me-pyridine-2-base 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph H H H H H H H H H H H H H Cl H H H H Cl H H Cl H H H H H H H H H H H H H H H H H H H H H H H H H B4 B7 H H H H H H H H H B7 B7 H H H H B1 B1 Cl CF 3 Cl Cl Cl Cl Me Me Me Cl Cl Cl Cl Cl OMe SMe CF 3 CF 3 CF 3 CF 3 Cl Cl Cl Cl H H H Cl H Me Cl H H H Cl Cl H H Me Cl Cl H Cl Cl Me Me H H H Me Me Me Me H Me CF 3 Me Me H H Me Me Me Me Me Me
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 3-F-Ph 3-F-Ph 3-F-Ph H Cl H H Cl H H H H H H Cl H H Cl H H H H H H Cl H H H H H H H H H H H H H H H H H H H H H H H H B3 B4 B6 B7 B7 B9 B20 B24 B2 B3 B4 B4 B6 B7 B7 B9 B20 B24 B6 B7 H H H Cl Cl Cl Cl Cl Cl Cl Cl CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Cl Cl Cl Cl CF 3 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl H H Cl Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me H H Me Me Me
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
3-F-Ph 4-F-Ph 4-F-Ph 4-F-Ph 4-F-Ph 2，3-F 2-Ph 2，3-F 2-Ph 2，4-F 2-Ph 2，4-F 2-Ph 2，5-F 2-Ph 2，5-F 2-Ph Ph Ph Ph Ph Ph Ph Ph Ph Ph Ph Ph Ph Cl H Cl H Cl H H H H H H H H H H H H H Cl H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B7 H H H H B7 B7 H H CF 3 Cl Cl CF 3 CF 3 Cl CF 3 Cl CF 3 Cl CF 3 Me Me Me Cl Cl Cl Cl Cl OMe SMe CF 3 CF 3 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl H Me Cl H H H Cl Cl H H Me Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me H Me CF 3 Me Me H H Me Me
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
Ph Ph Ph Ph Ph Ph Ph Ph Ph Ph Ph Ph Ph Ph Ph Ph Ph Ph Ph Ph Ph Ph Ph Cl H H Cl H Cl H H Cl H H H H H H Cl H H Cl H H H H H H H H H H H H H H H H H H H H H H H H H H H H B7 B1 B1 B3 B4 B6 B7 B7 B9 B20 B24 B2 B3 B4 B4 B6 B7 B7 B9 B20 B24 B6 CF 3 CF 3 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Cl Cl H Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl H Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me H
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
Ph 3，4-F 2-Ph 3，4-F 2-Ph 3，5-F 2-Ph 3，5-F 2-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph H H H H H H H H H H H H Cl H H H H Cl H H Cl H Cl H H H H H H H H H H H H H H H H H H H H H H H B7 H H H H H H H H H H H H H H H H H H B1 B1 B3 B4 Cl Cl CF 3 Cl CF 3 Me Me Me Cl Cl Cl Cl Cl OMe SMe CF 3 CF 3 CF 3 CF 3 Cl Cl Cl Cl H Cl Cl Cl Cl H Me Cl H H H Cl Cl H H Me Cl Cl H Cl Cl Cl Cl H Me Me Me Me Me Me Me H Me CF 3 Me Me H H Me Me Me Me Me Me Me Me
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 3-Cl-Ph 3-Cl-Ph 3-Cl-Ph 3-Cl-Ph 4-Cl-Ph H H Cl H H H H H H Cl H H Cl H H H H H H Cl H Cl H H H H H H H H H H H H H H H H H H H H H H H H B6 B7 B7 B9 B20 B24 B2 B3 B4 B4 B6 B7 B7 B9 B20 B24 B6 B7 H H H H H Cl Cl Cl Cl Cl Cl CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Cl Cl Cl Cl CF 3 CF 3 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl H H Cl Cl Cl Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me H H Me Me Me Me Me
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
4-Cl-Ph 4-Cl-Ph 4-Cl-Ph 2，3-Cl 2-Ph 2，3-Cl 2-Ph 2，4-Cl 2-Ph 2，4-Cl 2-Ph 2，5-Cl 2-Ph 2，5-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph Cl H Cl H H H H H H H H H H H H H Cl H H H H Cl H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B7 H H H H B7 B7 H H H H Cl CF 3 CF 3 Cl CF 3 Cl CF 3 Cl CF 3 Me Me Me Cl Cl Cl Cl Cl OMe SMe CF 3 CF 3 CF 3 CF 3 Cl Cl Cl Cl Cl Cl Cl Cl Cl H Me Cl H H H Cl Cl H H Me Cl Cl H Me Me Me Me Me Me Me Me Me Me Me Me H Me CF 3 Me Me H H Me Me Me Me
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 3，4-Cl 2-Ph H Cl H Cl H H Cl H H H H H H Cl H H Cl H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B1 B1 B3 B4 B6 B7 B7 B9 B20 B24 B2 B3 B4 B4 B6 B7 B7 B9 B20 B24 B8 B15 H Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl H H Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me H H Me
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
3，4-Cl 2-Ph 3，5-Cl 2-Ph 3，5-Cl 2-Ph 2-Me-Ph 2-Me-Ph 2，6-Me 2-Ph 2，6-Me 2-Ph 2-MeO-Ph 2-MeO-Ph 2-MeO-Ph 2-CF 3O-Ph 2-CF 3O-Ph 2-SMe-Ph 2-SMe-Ph 2-SOMe-Ph 2-SOMe-Ph 2-SO 2Me-Ph 2-SO 2Me-Ph 2-CF 3-Ph 2-CF 3-Ph 2-NO 2-Ph 2-NO 2-Ph 2-CN-Ph H H H H H H H H H Cl H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H CF 3 Cl CF 3 Cl CF 3 Cl CF 3 Cl CF 3 CF 3 Cl CF 3 Cl CF 3 Cl CF 3 Cl CF 3 Cl CF 3 Cl CF 3 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
2-CN-Ph 2-NHMe-Ph 2-NHMe-Ph 2-NMe 2-Ph 2-NMe 2-Ph 4-CH 2Ph-Ph 4-OPh-Ph 2-OH-Ph 2-OH-Ph 2-CO 2Me-Ph 2-CO 2Me-Ph 2-CO 2Et-Ph 2-CO 2Et-Ph H Cl Me Et nPr iPr iPr nBu nBu iBu H H H H H H H H H H H H H CO 2Et CO 2Et Ph Me H H H H H H H H H H H H H H H H H H H Ph H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H CF 3 Cl CF 3 Cl CF 3 Cl Cl Cl CF 3 Cl CF 3 Cl CF 3 Cl Cl Cl Cl Cl Cl CF 3 Cl CF 3 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
iBu iBu iBu secBu secBu 2，2-Me 2-propyl group nHex vinyl 1-acrylic 1-acrylic acetenyl 1-propynyl-11-propinyl CF3 CF 3 C 2F 5 C 2F 5 2，2-Cl 2-cPr 2，2-Cl 2-cPr cPr cPr 1-Me-cPr 1-Me-cPr H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B7 B7 H H H H H H H H H H H H H H H H H H H H CF 3 Cl CF 3 Cl CF 3 Cl Cl Cl Cl CF 3 Cl Cl CF 3 Cl CF 3 Cl CF 3 Cl CF 3 Cl CF 3 Cl CF 3 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
cHex cHex OMe OtBu OtBu OCF 3 OCF 3 StBu StBu SOtBu SOtBu SO 2tBu SO 2tBu NO 2 NO 2 CN CN NH 2 NH 2 NHMe NHMe NMe 2 NMe 2 H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H Cl CF 3 Cl Cl CF 3 Cl CF 3 Cl CF 3 Cl CF 3 Cl CF 3 Cl CF 3 Cl CF 3 Cl CF 3 Cl CF 3 Cl CF 3 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
CH 2Ph H CH 2Ph H OPh H OPh H OH H OH H naphthyl-1 H naphthyl-1 H naphthyl-2 H naphthyl-2 H CO2Me H CO 2Me H CO 2Et H CO 2Et H 2-thienyl H 2-thienyl H CH 2OMe H COCH 3 H -N＝CMe 2 H -N＝CMe 2 H -(CH 2) 3- -(CH 2) 3- -(CH 2) 4- H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H Cl CF 3 Cl CF 3 Cl CF 3 Cl CF 3 Cl CF 3 Cl CF 3 Cl CF 3 Cl CF 3 Cl Cl Cl CF 3 Cl CF 3 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 1 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
-(CH 2) 4- H H CF 3 Cl Me
Table 2
Figure C9719404101341
Table 2 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph H H H H H Cl H H H H H Me Cl H Me H Cl CF 3 OMe NH 2 NHMe NMe 2 NO 2 H H H H H H H H H H H H H H H Cl H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H Me Me Me Me Me Me Et Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl H H H Me Cl Cl Me Me H H H H H Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me CF 3 H Me Me Me Me Me Me CF 3 H H H Me Me Me Me Me Me Me Me Me Me
Table 2 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph CN OH CO 2Me CO 2Et H H H H H H H H H H H H H Me Cl Br CF 3 NO 2 CN H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H Cl Cl Cl Cl Cl Cl Cl Cl Cl Br Me Me OMe OCF 3 SMe CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Cl Cl Cl Cl Cl Cl Cl Cl CF 3 Me Br OMe H H H Me Cl Cl Cl Cl Cl Cl Cl Me Me Me Me CF 3 CF 2H CH 2OMe COMe Me Me Me Me H H H Me Me Me Me Me Me Me Me
Table 2 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph CO 2Me CO 2Et H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B1 B2 B3 B4 B5 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Cl Cl CO 2Me Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl H Br NO 2 CN NHMe NMe 2 CO 2Me OMe OCF 2H NO 2 CN Me Cl Cl Cl Cl Cl Me Me CF 3 CF 2H CH 2OMe COCH 3 Me Me Me Me Me Me Me Me CF 2H Me Me Me Me Me Me Me Me
Table 2 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B6 B7 B8 B9 B10 B11 B12 B13 B14 B15 B16 B17 B18 B19 B20 B21 B22 B23 B24 B25 B26 B27 B28 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 2 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B29 B30 B31 B32 B33 B34 Na K B2 B3 B4 B5 B6 B7 B8 B9 B10 B11 B12 B13 B14 B15 B16 Cl Cl Cl Cl Cl Cl Cl Cl CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 2 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B17 B18 B19 B20 B21 B22 B23 B24 B25 B26 B27 B28 B29 B30 B31 B32 B33 B34 Na K B7 B9 B10 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl H H H Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me H H H
Table 2 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
2，6-F 2-PhPh tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu H H H H H H Cl H H H H H Me Cl NO 2 CO 2Me CO 2Et H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B11 H H H H H H H H H H H H H H H H H H H H H H Cl Me Me Me Me Me Me Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Br H H H H Me Cl Cl Me H H H Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl CF 3 Me H Me CF 3 H Me Me Me Me Me CF 3 H Me Me Me Me Me Me CF 3 CF 2H CH 2OMe COMe Me Me
Table 2 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu H H H H Me Cl NO 2 CO 2Me CO 2Et H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H Me OMe CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 NO 2 CN CN Cl CO 2Me CO 2Me Br H Me Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl H NO 2 NHMe NMe 2 Me Cl Me CN Me Cl Me H Me Me Me Me Me Me Me CF 3 CF 2H CH 2OMe COCH 3 Me Me Me Me Me Me Me Me Me Me
Table 2 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu H Cl H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B1 B1 B2 B3 B4 B5 B6 B7 B8 B9 B10 B11 B12 B13 B14 B15 B16 B17 B18 B19 B20 B21 B22 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 2 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B23 B24 B25 B26 B27 B28 B29 B30 B31 B32 B33 B34 Na K B2 B3 B4 B5 B6 B7 B8 B9 B10 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 2 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B11 B12 B13 B14 B15 B16 B17 B18 B19 B20 B21 B22 B23 B24 B25 B26 B27 B28 B29 B30 B31 B32 B33 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 2 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
TBu tBu tBu tBu tBu tBu tBu tBu tBu 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals H H H H H H H H H H H H H H H H H H Cl CO 2Me CO 2Et H H H H H H H H H H H H H H H H H H H H H H H H H B34 Na K B7 B8 B15 B17 B18 B34 H H B7 H H H H H H H H H H H CF 3 CF 3 CF 3 Cl Cl Cl Cl Cl Cl Me Me Me Me Me Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl H H H H H H H H H Me Cl Me H H H H H H Cl CF 3 Me Me Me H H H H H H Me CF 3 H Me Me Me Me CF 3 H H H H Me Me
Table 2 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B7 H H H B7 B1 B3 B7 B3 B7 B3 B4 B5 B6 B7 B8 B9 B10 B11 B15 B16 Br Me OMe CF 3 CF 3 CF 3 CF 3 Cl Cl Cl CF 3 CF 3 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Br H Me Cl H H Cl Cl Cl Cl Cl H H H H H H H H H H H Me Me H Me Me Me H Me Me Me Me Me H H H H H H H H H H H
Table 2 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 3-pyridine radicals 3-pyridine radicals 4-pyridine radicals 4-pyridine radicals 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph H H H H H H H H H H H H H H H H H H H H Cl H H H H H H H H H H H H H H H H H H H H H H H H H B17 B28 B30 B31 B32 B34 H H H H H H B7 B7 H H B1 B3 B6 B7 B7 B3 B6 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl OMe SMe CF 3 CF 3 Cl Cl Cl Cl Cl CF 3 CF 3 H H H H H H Cl H Cl H H Cl H H Cl H Cl Cl Cl Cl Cl Cl Cl H H H H H H Me H Me H H Me H H Me Me Me Me Me Me Me Me Me
Table 2 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
2-F-Ph 2-F-Ph 2-F-Ph 3-F-Ph 3-F-Ph 4-F-Ph 4-F-Ph 2，3-F 2-Ph 2，4-F 2-Ph 2，5-F 2-Ph Ph Ph Ph Ph Ph Ph Ph Ph Ph Ph Ph Ph Ph H Cl H H H H H H H H H H H H H H H H H H Cl H H H H H H H H H H H H H H H H H H H H H H H H H B7 B7 B7 H H H H H H H H H H H H H B1 B3 B6 B7 B7 B3 B6 CF 3 CF 3 Cl Cl CF 3 Cl CF 3 Cl Cl Cl Cl Cl OMe SMe CF 3 CF 3 Cl Cl Cl Cl Cl CF 3 CF 3 Cl Cl H Cl Cl Cl Cl Cl Cl Cl H Cl H H Cl H Cl Cl Cl Cl Cl Cl Cl Me Me H Me Me Me Me Me Me Me H Me H H Me Me Me Me Me Me Me Me Me
Table 2 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
Ph Ph Ph Ph Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 3-Cl-Ph 4-Cl-Ph H Cl H H H H H H H H H H H H H Cl H H H Cl H H H H H H H H H H H H H H H H H H H H H H H H H H B7 B7 B7 H H H H H H H H B1 B3 B6 B7 B7 B3 B6 B7 B7 B7 H H CF 3 CF 3 Cl Cl Cl Cl Cl OMe SMe CF 3 CF 3 Cl Cl Cl Cl Cl CF 3 CF 3 CF 3 CF 3 Cl Cl Cl Cl Cl H Cl Cl H Cl H H Cl H Cl Cl Cl Cl Cl Cl Cl Cl Cl H Cl Cl Me Me H Me Me H Me H H Me Me Me Me Me Me Me Me Me Me Me H Me Me
Table 2 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
2，3-Cl 2-Ph 2，4-Cl 2-Ph 2，5-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 3，4-Cl 2-Ph 3，5-Cl 2-Ph 2-Me-Ph 2-Me-Ph H H H H H H H H H H H H H Cl H H H Cl H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B1 B3 B6 B7 B7 B3 B6 B7 B7 B7 H H H H Cl Cl Cl Cl Cl OMe SMe CF 3 CF 3 Cl Cl Cl Cl Cl CF 3 CF 3 CF 3 CF 3 Cl Cl Cl Cl CF 3 Cl Cl Cl H Cl H H Cl H Cl Cl Cl Cl Cl Cl Cl Cl Cl H Cl Cl Cl Cl Me Me Me H Me H H Me Me Me Me Me Me Me Me Me Me Me H Me Me Me Me
Table 2 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
2，6-Me 2-Ph 2，6-Me 2-Ph 2-MeO-Ph 2-MeO-Ph 2-CF 3O-Ph 2-SMe-Ph 2-SOMe-Ph 2-SO 2Me-Ph 2-CF 3-Ph 2-NO 2-Ph 2-CN-Ph 2-NHMe-Ph 2-NMe 2-Ph 4-benzyl-Ph 4-phenoxy group-Ph 2-OH-Ph 2-CO 2Me-Ph 2-CO 2Et-Ph H Me Et nPr iPr H H H H H H H H H H H H H H H H H H CO 2Et Ph Me H H H H H H H H H H H H H H H H H H H H Ph H H H H H H H H H H H H H H H H H H H H H H H H H H H Cl CF 3 Cl CF 3 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 2 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
iPr nBu nBu iBu iBu iBu iBu iBu secBu secBu 2，2-Me 2-propyl group nHex vinyl 1-acrylic 1-acrylic acetenyl 1-propinyl CF3 CHF 2 C 2F 5 2，2-Cl 2-cPr 2，2-Cl 2-cPr cPr H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B7 B7 H H H H H H H H H H H H H H H H CF 3 Cl CF 3 Cl CF 3 Cl CF 3 Cl Cl CF 3 Cl Cl Cl Cl CF 3 Cl Cl Cl Cl Cl Cl CF 3 Cl Cl Cl Cl Cl Cl Cl Cl H Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me Me Me Me Me Me H Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 2 (continuing)
R 1 R 2 R 3 B Y 1 Y 2 Y 3
cPr 1-Me-cPr 1-Me-cPr cHex cHex CH 2Ph naphthyl-1 naphthyl-1 naphthyl-2 CO 2Me CO 2Et 2-thienyl CH 2OMe CH 2OEt COCH 3 COtBu H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H CF 3 Cl CF 3 Cl CF 3 Cl Cl CF 3 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 3
Figure C9719404101551
R 1 R 2 R 3 B Y 1 Y 2
2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph H H Me Cl H H H H H H H H H H H H H H H H H H Cl H H H H Cl H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B3 B6 B7 B7 Me Et Et Et Et Cl Cl Cl Me Br Me Me OMe OCF 3 SMe CO 2Me CO 2Et CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Me Me Me Me Me Cl Me CF 3 Cl Me Br CF 3 Me Me Me Me Me Me H Me Me Me Me
Table 3 (continuing)
R 1 R 2 R 3 B Y 1 Y 2
tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu H H H H H H H H H H H H H H H Me Cl Br CF 3 NO 2 CN CO 2Me CO 2Et H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H Me Et Cl Cl Me Cl Br Me Me OMe OCF 3 SMe CO 2Me CO 2Et CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Me Me Cl Me Cl CF 3 Me Br CF 3 Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 3 (continuing)
R 1 R 2 R 3 B Y 1 Y 2
tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu H H H H H H H H H H H H H Cl H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B2 B3 B4 B5 B6 B7 B7 B8 B9 B10 B11 B12 B13 B14 B15 B16 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 H Br NO 2 CN NHMe NMe 2 CO 2Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 3 (continuing)
R 1 R 2 R 3 B Y 1 Y 2
TBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B17 B18 B19 B20 B21 B22 B23 B24 B25 B26 B27 B28 B29 B30 B31 B32 B33 B34 Na K H H H CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Me Et Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Cl
Table 3 (continuing)
R 1 R 2 R 3 B Y 1 Y 2
2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 3-pyridine radicals 4-pyridine radicals 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B3 B6 B7 H H H H H H H Cl Cl Me Br Me Me OMe OCF 3 SMe CO 2Me CO 2Et CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Me Et CF 3 CF 3 CF 3 Me CF 3 Cl Me Br CF 3 Me Me Me Me Me Me H Me Me Me Me Me Me Me Me Cl H
Table 3 (continuing)
R 1 R 2 R 3 B Y 1 Y 2
2-F-Ph 2-F-Ph 2-F-Ph 3-F-Ph 4-F-Ph 2，3-F 2-Ph 2，4-F 2-Ph 2，5-F 2-Ph Ph Ph Ph Ph Ph Ph Ph Ph 3，4-F 2-Ph 3，5-F 2-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B3 B6 B7 H H H H H H H H H H B3 B6 B7 H H H H H H H CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Me Et CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Me Et CF 3 CF 3 CF 3 Me Me Me Me Me Me Me Me Me Me Me Cl H Me Me Me Me Me Me Me Me Cl H
Table 3 (continuing)
R 1 R 2 R 3 B Y 1 Y 2
2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 3-Cl-Ph 4-Cl-Ph 2，3-Cl 2-Ph 2，4-Cl 2-Ph 2，5-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 3，4-Cl 2-Ph 3，5-Cl 2-Ph 2-Me-Ph 2，6-Me 2-Ph 2-MeO-Ph 2-CF 3O-Ph 2-SMe-Ph H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B3 B6 B7 H H H H H H H H H H B3 B6 B7 H H H H H H H CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Me Et CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Me Me Me Me Me Me Me Me Me Me Me Cl H Me Me Me Me Me Me Me Me Me Me
Table 3 (continuing)
R 1 R 2 R 3 B Y 1 Y 2
2-SOMe-Ph 2-SO 2Me-Ph 2-CF 3-Ph 2-NO 2-Ph 2-CN-Ph 2-NHMe-Ph 2-NMe 2-Ph 4-benzyl-Ph 4-phenoxy group-Ph 2-OH-Ph 2-CO 2Me-Ph 2-CO 2Et-Ph H Me Et nPr iPr iPr nBu nBu iBu iBu iBu H H H H H H H H H H H H CO 2Et Ph Me H H H H H H H H H H H H H H H H H H H H Ph H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B7 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Et CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Et CF 3 Et CF 3 Et CF 3 Et Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 3 (continuing)
R 1 R 2 R 3 B Y 1 Y 2
iBu secBu secBu 2，2-Me 2-propyl group nHex vinyl 1-acrylic acetenyl 1-propinyl CF3 CHF 2 C 2F 5 2，2-Cl 2-cPr 2，2-Cl 2-cPr cPr cPr 1-Me-cPr 1-Me-cPr cHex cHex CH 2Ph naphthyl 1-1 naphthyl 1-1 H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B7 H H H H H H H H H H H H H H H H H H H H H H CF 3 Et CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Et CF 3 Et CF 3 Et CF 3 Et CF 3 CF 3 Et CF 3 Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 3 (continuing)
R 1 R 2 R 3 B Y 1 Y 2
Naphthyl-2 CO 2Me CO 2Et 2-thienyl CH 2OMe CH 2OEt COCH 3 COtBu COPh H H H H H H H H H H H H H H H H H H H H H H H H H H H CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Me Me Me Me Me Me Me Me Me
Table 4
Figure C9719404101671
Figure C9719404101681
Figure C9719404101701
R 1 R 2 B Y 1 Y 2 Y 3
2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph H H H H H H H H H H H H H H H H H H H H H H H H H H B7 H H H H H H H H H H H H H H H H B7 B7 B7 H Me Me Me Me Me Me Et Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Br Me OMe OCF 3 SMe CF 3 H H H Me Cl Br Me Me H H H Cl Cl Cl Cl Cl CF 3 Me OMe H H H Me Me CF 3 H Me Me Me Me Me Me CF 3 H Me CF 3 CF 2H CH 2OMe COMe Me Me Me H H H
Table 4 (continuing)
R 1 R 2 B Y 1 Y 2 Y 3
2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B1 B3 B6 B7 B2 B3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Cl Cl CO 2Me Cl Cl Cl Cl CF 3 CF 3 Me Cl Cl Cl Cl H Br NO 2 CN NHMe NMe 2 CO 2Me OMe OCF 2H NO 2 CN Me Cl Cl Cl Cl Cl Cl Me Me CF 3 CF 2H CH 2OMe Me Me Me Me Me Me Me Me CF 2H Me Me Me Me Me Me Me Me Me
Table 4 (continuing)
R 1 R 2 B Y 1 Y 2 Y 3
2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph H H H H H H H H H H H H H H H H H H H H H H H B4 B5 B6 B7 B8 B9 B10 B11 B12 B13 B14 B15 B16 B17 B18 B19 B20 B21 B22 B23 B24 B25 B26 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 4 (continuing)
R 1 R 2 B Y 1 Y 2 Y 3
2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph tBu tBu tBu tBu tBu tBu tBu tBu tBu H H H H H H H H H H H H H H H H H H H H H H H B27 B28 B29 B30 B31 B32 B33 B34 Na K B7 B9 B10 B11 H H H B7 H H H H H CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Cl Cl Cl Cl H Me Me Me Me Me Me Et Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl H H H H CF 3 H H H Me Cl Br Me Me Me Me Me Me Me Me Me Me Me Me H H H H Me Me CF 3 H Me Me Me Me Me
Table 4 (continuing)
R 1 R 2 B Y 1 Y 2 Y 3
tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu H H H Me Cl H H H H H H H H H H H H H Br CF 3 NO 2 CN CO 2Me H H H H H H H H H H H H H B7 B7 B7 H H H H H H H Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Br Me OMe OCF 3 SMe CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 H H H H H Cl Cl Cl Cl Cl CF 3 Me OMe H H H Me Cl Cl Cl Cl Cl Cl Me CF 3 H H H Me CF 3 CF 2H CH 2OMe COMe Me Me Me H H H Me Me Me Me Me Me Me
Table 4 (continuing)
R 1 R 2 B Y 1 Y 2 Y 3
tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu CO 2Et H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B1 B2 B3 B4 B5 B6 B7 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Cl Cl CO 2Me Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl H Br NO 2 CN NHMe NMe 2 CO 2Me OMe OCF 2H NO 2 CN Me Cl Cl Cl Cl Cl Cl Cl Me CF 3 CF 2H CH 2OMe Me Me Me Me Me Me Me Me CF 2H Me Me Me Me Me Me Me Me Me Me
Table 4 (continuing)
R 1 R 2 B Y 1 Y 2 Y 3
tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu H H H H H H H H H H H H H H H H H H H H H H H B8 B9 B10 B11 B12 B13 B14 B15 B16 B17 B18 B19 B20 B21 B22 B23 B24 B25 B26 B27 B28 B29 B30 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 4 (continuing)
R 1 R 2 B Y 1 Y 2 Y 3
tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu H H H H H H H H H H H H H H H H H H H H H H H B31 B32 B33 B34 Na K B2 B3 B4 B5 B6 B7 B8 B9 B10 B11 B12 B13 B14 B15 B16 B17 B18 Cl Cl Cl Cl Cl Cl CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 4 (continuing)
R 1 R 2 B Y 1 Y 2 Y 3
TBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu 2-pyridine radicals H H H H H H H H H H H H H H H H H H H H H H H B19 B20 B21 B22 B23 B24 B25 B26 B27 B28 B29 B30 B31 B32 B33 B34 Na K B7 B8 B15 B34 H CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Cl Cl Cl Cl H Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl H H H H CF 3 Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me H H H H Me
Table 4 (continuing)
R 1 R 2 B Y 1 Y 2 Y 3
2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals H H H H H H H H H H H Me Cl H H H H H H H H H H H H B7 H H H H H H H H H H H H H H H H H H H H Me Me Me Me Me Me Et Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Br Me Br OMe H H H Me Cl Br Me Me H H H H H Cl Cl Cl Cl Cl CF 3 Me OMe H H Me CF 3 H Me Me Me Me Me Me CF 3 H H H Me CF 3 CF 2H CH 2OMe COMe Me Me Me H H
Table 4 (continuing)
R 1 R 2 B Y 1 Y 2 Y 3
2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals H H H H H H H H H H H H H H H H H H H H H H H B7 B7 B7 B7 B7 B7 B7 B7 B7 H H H H H H H H B3 B6 B7 B3 B6 B7 OCF 3 SMe NH 2 NHMe NMe 2 NO 2 CN CO 2Me CO 2Et CF 3 CF 3 CF 3 CF 3 CF 3 Cl Cl CO 2Me Cl Cl Cl CF 3 CF 3 CF 3 H H H H H H H H H Me Cl H Br CO 2Me NO 2 CN Me Cl Cl Cl Cl Cl Cl H H H H H H H H H Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 4 (continuing)
R 1 R 2 B Y 1 Y 2 Y 3
2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals H H H H H H H H H H H H H H H H H H H H H H H B2 B3 B4 B5 B6 B7 B8 B9 B10 B11 B12 B13 B14 B15 B16 B17 B18 B19 B20 B21 B22 B23 B24 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H
Table 4 (continuing)
R 1 R 2 B Y 1 Y 2 Y 3
2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 3-pyridine radicals 3-pyridine radicals 3-pyridine radicals 4-pyridine radicals 4-pyridine radicals 4-pyridine radicals 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph H H H H H H H H H H H H H H H H H H H H H H H B25 B26 B27 B28 B29 B30 B31 B32 B33 B34 Na K H H H H H H H H H H H Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl CF 3 Cl Cl CF 3 Cl Me Me Cl Cl Cl H H H H H H H H H H H H Cl Cl H Cl Cl H Me Cl Me H Cl H H H H H H H H H H H H Me Me H Me Me H Me Me Me H Me
Table 4 (continuing)
R 1 R 2 B Y 1 Y 2 Y 3
2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 3-F-Ph 4-F-Ph 2，3-F 2-Ph 2，4-F 2-Ph 2，5-F 2-Ph Ph Ph Ph Ph Ph Ph H H H H H H H H H H H H H H H H H H H H H H H B7 B7 B7 B7 B1 B3 B6 B7 B3 B6 B7 B7 H H H H H H H H H H B7 OMe SMe CF 3 CF 3 Cl Cl Cl Cl CF 3 CF 3 CF 3 Cl Cl Cl Cl Cl Cl Me Me Cl Cl Cl OMe H H Cl H Cl Cl Cl Cl Cl Cl Cl H Cl Cl Cl Cl Cl Me Cl Me H Cl H H H Me Me Me Me Me Me Me Me Me H Me Me Me Me Me Me Me Me H Me H
Table 4 (continuing)
R 1 R 2 B Y 1 Y 2 Y 3
Ph Ph Ph Ph Ph Ph Ph Ph Ph Ph Ph Ph 3，4-F 2-Ph 3，5-F 2-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph H H H H H H H H H H Me H H H H H H H H H H H H B7 H H B1 B3 B6 B7 B3 B6 B7 B7 B7 H H H H H H H H H H H SMe CF 3 CF 3 Cl Cl Cl Cl CF 3 CF 3 CF 3 CF 3 Cl Cl Cl Me Me Cl Cl Cl OMe SMe CF 3 CF 3 H Cl H Cl Cl Cl Cl Cl Cl Cl Cl H Cl Cl Me Cl Me H Cl H H Cl H H Me Me Me Me Me Me Me Me Me Me H Me Me Me Me Me H Me H H Me Me
Table 4 (continuing)
R 1 R 2 B Y 1 Y 2 Y 3
2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 3-Cl-Ph 4-Cl-Ph 2，3-Cl 2-Ph 2，4-Cl 2-Ph 2，5-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph H H H H H H H H H H H H H H H H H H H H H H H B1 B3 B6 B7 B3 B6 B7 B7 H H H H H H H H H H B7 B7 H H B1 Cl Cl Cl Cl CF 3 CF 3 CF 3 Cl Cl Cl Cl Cl Cl Me Me Cl Cl Cl OMe SMe CF 3 CF 3 Cl Cl Cl Cl Cl Cl Cl Cl H Cl Cl Cl Cl Cl Me Cl Me H Cl H H Cl H Cl Me Me Me Me Me Me Me H Me Me Me Me Me Me Me Me H Me H H Me Me Me
Table 4 (continuing)
R 1 R 2 B Y 1 Y 2 Y 3
2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 3，4-Cl 2-Ph 3，5-Cl 2-Ph 2-Me-Ph 2-Me-Ph 2，6-Me 2-Ph 2，6-Me 2-Ph 2-MeO-Ph 2-MeO-Ph 2-CF 3O-Ph 2-CF 3O-Ph 2-SMe-Ph 2-SMe-Ph 2-SOMe-Ph 2-SOMe-Ph H H H Cl H H H Cl H H H H H H H H H H H H H H H B3 B6 B7 B7 B3 B6 B7 B7 B7 H H H H H H H H H H H H H H Cl Cl Cl Cl CF 3 CF 3 CF 3 CF 3 Cl Cl Cl Cl CF 3 Cl CF 3 Cl CF 3 Cl CF 3 Cl CF 3 Cl CF 3 Cl Cl Cl Cl Cl Cl Cl Cl H Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me Me Me Me Me Me Me H Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 4 (continuing)
R 1 R 2 B Y 1 Y 2 Y 3
2-SO 2Me-Ph 2-SO 2Me-Ph 2-CF 3-Ph 2-CF 3-Ph 2-NO 2-Ph 2-NO 2-Ph 2-CN-Ph 2-CN-Ph 2-NHMe-Ph 2-NMe 2-Ph 4-benzyl-Ph 4-phenoxy group-Ph 2-OH-Ph 2-CO 2Me-Ph 2-CO 2Me-Ph 2-CO 2Et-Ph 2-CO 2Et-Ph H Me Et nPr iPr iPr H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H Cl CF 3 Cl CF 3 Cl CF 3 Cl CF 3 Cl Cl Cl Cl Cl Cl CF 3 Cl CF 3 Cl Cl Cl Cl Cl CF 3 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 4 (continuing)
R 1 R 2 B Y 1 Y 2 Y 3
nBu nBu iBu iBu iBu iBu iBu secBu secBu 2，2-Me 2-propyl group nHex vinyl 1-acrylic 1-acrylic acetenyl 1-propinyl CF3 CF 3 CHF 2 C 2F 5 2，2-Cl 2-cPr 2，2-Cl 2-cPr cPr H H H H H H H H H H H H H H H H H H H H H H H H H H H B7 B7 H H H H H H H H H H H H H H H H H Cl CF 3 Cl CF 3 Cl CF 3 Cl Cl CF 3 Cl Cl Cl Cl CF 3 Cl Cl Cl CF 3 Cl Cl Cl CF 3 Cl Cl Cl Cl Cl Cl Cl H Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me Me Me Me Me H Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 4 (continuing)
R 1 R 2 B Y 1 Y 2 Y 3
cPr 1-Me-cPr 1-Me-cPr cHex cHex CH 2Ph naphthyl-1 naphthyl-1 naphthyl-2 CO 2Me CO 2Et 2-thienyl 2-thienyl CH 2OMe CH 2OEt COCH 3 COtBu COPh H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H CF 3 Cl CF 3 Cl CF 3 Cl Cl CF 3 Cl Cl Cl Cl CF 3 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 5
Figure C9719404101911
Figure C9719404101931
R 1 R 2 B Y 1 Y 2
2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph H H H Me H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H Me Me Et Et Cl Cl Cl Me Br Me OMe OCF 3 SMe CO 2Me CO 2Et CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 H Me Me Me Cl Me CF 3 Cl Me CF 3 Me Me Me Me Me Me H Br NO 2 CN NHMe NMe 2 CO 2Me
Table 5 (continuing)
R 1 R 2 B Y 1 Y 2
2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu H H H H H H H H H H H H H H H H H H H H H H H B3 B6 B7 H H H H H H H H H H H H H H H H H H B2 B3 CF 3 CF 3 CF 3 Me Et Cl Cl Me Cl Br Me Me OMe OCF 3 SMe CO 2Me CO 2Et CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Me Me Me Me Me Cl Me Cl CF 3 Me Br CF 3 Me Me Me Me Me Me H Br NO 2 Me Me
Table 5 (continuing)
R 1 R 2 B Y 1 Y 2
TBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu 2-pyridine radicals H H H H H H H H H H H H H H H H H H H H H H H B4 B5 B6 B7 B8 B9 B10 B11 B14 B20 B23 B24 B25 B26 B28 B30 B31 B32 B33 B34 Na K H CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 5 (continuing)
R 1 R 2 B Y 1 Y 2
2-pyridyl 2-pyridyl 2-pyridyl 2-pyridyl 2-pyridyl 2-pyridyl 2-pyridyl 2-pyridyl 2-pyridyl 2-pyridyl 2-pyridyl 2-pyridyl 2-pyridyl 2-pyridyl 2-pyridyl 2-pyridyl 3-pyridyl 3-pyridyl 4-pyridyl 4-pyridyl 2-F-Ph 2-F-Ph 2-F-Ph H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B3 B6 B7 H H H H H H H Et Cl Cl Me Br Me CO 2Me CO 2Et CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Et CF 3 Et CF 3 Me Et CF 3 Me Cl Me Cl Me CF 3 Me Me Me Br NO 2 CN NMe 2 Me Me Me Me Me Me Me Me Me Me
Table 5 (continuing)
R 1 R 2 B Y 1 Y 2
2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 3-F-Ph 3-F-Ph 4-F-Ph 2，3-F 2-Ph 2，4-F 2-Ph 2，5-F 2-Ph Ph Ph Ph Ph Ph Ph Ph Ph 3，4-F 2-Ph 3，5-F 2-Ph 2-Cl-Ph 2-Cl-Ph H H H H H H H H H H H H H H H H H H H H H H H H H B3 B6 B7 H H H H H H H H H H H B3 B6 B7 H H H H CF 3 CF 3 CF 3 CF 3 CF 3 Et CF 3 Et Et Et Et Me Et CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Et Et Me Et Cl H Me Me Me Me Me Me Me Me Me Me Me Me Cl H Me Me Me Me Me Me Me
Table 5 (continuing)
R 1 R 2 B Y 1 Y 2
2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 3-Cl-Ph 4-Cl-Ph 2，3-Cl 2-Ph 2，4-Cl 2-Ph 2，5-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 3，4-Cl 2-Ph 3，5-Cl 2-Ph 2-Me-Ph 2-Me-Ph H H H H H H H H H H H H H H H H H H H H H H H H H H B3 B6 B7 H H H H H H H H H H B3 B6 B7 H H H H CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Me Et CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Et CF 3 Me Cl H Me Me Me Me Me Me Me Me Me Me Me Cl H Me Me Me Me Me Me Me
Table 5 (continuing)
R 1 R 2 B Y 1 Y 2
2，6-Me 2-Ph 2，6-Me 2-Ph 2-MeO-Ph 2-MeO-Ph 2-CF 3O-Ph 2-CF 3O-Ph 2-SMe-Ph 2-SMe-Ph 2-SOMe-Ph 2-SOMe-Ph 2-SO 2Me-Ph 2-SO 2Me-Ph 2-CF 3-Ph 2-CF 3-Ph 2-NO 2-Ph 2-NO 2-Ph 2-CN-Ph 2-NHMe-Ph 2-NMe 2-Ph 2-NMe 2-Ph 4-benzyl-Ph 4-phenoxy group-Ph 2-OH-Ph H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H Et CF 3 Et CF 3 Et CF 3 Et CF 3 Et CF 3 Et CF 3 Et CF 3 Et CF 3 Et CF 3 Et CF 3 CF 3 CF 3 CF 3 Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 5 (continuing)
R 1 R 2 B Y 1 Y 2
2-CO 2Me-Ph 2-CO 2Me-Ph 2-CO 2Et-Ph 2-CO 2Et-Ph H Me Et nPr iPr iPr nBu nBu iBu iBu iBu iBu secBu secBu 2，2-Me 2-propyl group nHex vinyl 1-propenyl 1-propenyl H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H B7 B7 H H H H H H H Et CF 3 Et CF 3 CF 3 CF 3 CF 3 CF 3 Et CF 3 Et CF 3 Et CF 3 Et CF 3 Et CF 3 CF 3 CF 3 CF 3 Et CF 3 Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 5 (continuing)
R 1 R 2 B Y 1 Y 2
Ethynyl 1-proyl CF 3 CF 3 CHF 2 C 2F 5 2，2-Cl 2-cPr 2，2-Cl 2-cPr cPr cPr 1-Me-cPr 1-Me-cPr cHex cHex CH 2Ph 1-naphthyl 1-naphthyl 2-naphthyl CO 2Me CO 2Et 2-thienyl H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H CF 3 CF 3 Et CF 3 Et Et Et CF 3 Et CF 3 Et CF 3 Et CF 3 CF 3 Et CF 3 CF 3 CF 3 CF 3 CF 3 Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 6
R 1 R 2 B Y 1 Y 2 Y 3
2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph H H H H H H H H H H H H H H H H H H H H H H H B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 H Me Me Me Me Me Me Et Cl Cl Cl Cl Cl Cl Cl Cl Cl Br Me OMe OCF 3 SMe CF 3 CF 3 H H H Me Cl Br Me Me H H H Cl Cl Cl Cl CF 3 Me OMe H H H Me Me Me CF 3 H Me Me Me Me Me Me CF 3 H CF 3 CF 2H CH 2OMe COMe Me Me Me H H H Me
Table 6 (continuing)
R 1 R 2 B Y 1 Y 2 Y 3
2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph H H H H H H H H H H H H H H H H Me H H H H H Me B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B1 B1 B3 B4 B5 B6 B7 B7 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Cl Cl CO 2Me Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl H Br NO 2 CN NHMe NMe 2 CO 2Me OMe OCF 2H NO 2 CN Me Cl Cl Cl Cl Cl Cl Cl Cl CF 3 CF 2H CH 2OMe Me Me Me Me Me Me Me Me CF 2H Me Me Me Me Me Me Me Me Me Me Me
Table 6 (continuing)
R 1 R 2 B Y 1 Y 2 Y 3
2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph H H H H H H Me H H H H H H H H H H H H H H H H B2 B3 B4 B5 B6 B7 B7 B8 B9 B10 B11 B12 B13 B14 B15 B16 B17 B18 B19 B20 B21 B22 B23 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 6 (continuing)
R 1 R 2 B Y 1 Y 2 Y 3
2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph tBu tBu tBu tBu tBu tBu H H H H H H H H H H H H H H H H H H H H H H H B24 B25 B26 B27 B28 B29 B30 B31 B32 B33 B34 B7 B9 B10 B11 B45 B46 B7 B7 B7 B7 B7 B7 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Cl Cl Cl Cl CF 3 CF 3 H Me Me Me Me Me Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl H H H H Cl Cl CF 3 H H H Me Cl Me Me Me Me Me Me Me Me Me Me Me H H H H Me Me Me Me CF 3 H Me Me
Table 6 (continuing)
R 1 R 2 B Y 1 Y 2 Y 3
tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu H H H H H H H H H H H H H H H H H Br Me CF 3 NO 2 CN CO 2Me B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 Me Et Cl Cl Cl Cl Cl Cl C1 Cl Cl Br Me OMe OCF 3 SMe CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Br Me Me H H H Cl Cl Cl Cl CF 3 Me OMe H H H Me Cl Cl Cl Cl Cl Cl Me Me Me Me CF 3 H CF 3 CF 2H CH 2OMe COMe Me Me Me H H H Me Me Me Me Me Me Me
Table 6 (continuing)
R 1 R 2 B Y 1 Y 2 Y 3
tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu CO 2Et H H H H H H H H H H H H H H H H H H H H H H B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B1 B2 B3 B4 B5 B6 B7 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Cl Cl CO 2Me Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl H Br NO 2 CN NHMe NMe 2 CO 2Me OMe OCF 2H NO 2 CN Me Cl Cl Cl Cl Cl Cl Cl Me CF 3 CF 2H CH 2OMe Me Me Me Me Me Me Me Me CF 2H Me Me Me Me Me Me Me Me Me Me
Table 6 (continuing)
R 1 R 2 B Y 1 Y 2 Y 3
tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu Me H H H H H H H H H H H H H H H H H H H H H H B7 B8 B9 B10 B11 B12 B13 B14 B15 B16 B17 B18 B19 B20 B21 B22 B23 B24 B25 B26 B27 B28 B29 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 6 (continuing)
R 1 R 2 B Y 1 Y 2 Y 3
tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu H H H H H H H H H H H H H H H H H H H H H H H B30 B31 B32 B33 B34 B45 B46 B2 B3 B4 B5 B6 B7 B8 B9 B10 B11 B12 B13 B14 B15 B16 B17 Cl Cl Cl Cl Cl Cl Cl CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 6 (continuing)
R 1 R 2 B Y 1 Y 2 Y 3
tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu H H H H H H H H H H H H H H H H H H H H H H H B18 B19 B20 B21 B22 B23 B24 B25 B26 B27 B28 B29 B30 B31 B32 B33 B34 B35 B43 B7 B9 B10 B11 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl H H H H Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me H H H H
Table 6 (continuing)
R 1 R 2 B Y 1 Y 2 Y 3
2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals H H H H H H H H H H H H H H H H H H H H H H H B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B3 B7 B3 B7 B3 B4 H Me Me Me Me Me Cl Cl OMe OCF 3 SMe NO 2 CO 2Me CO 2Et CF 3 CF 3 CF 3 Cl Cl CF 3 CF 3 Cl Cl CF 3 H H H Me Cl H H H H H H H H Me H Br Cl Cl Cl Cl H H Me Me CF 3 H Me Me Me CF 3 H H H H H H Me Me Me Me Me Me Me H H
Table 6 (continuing)
R 1 R 2 B Y 1 Y 2 Y 3
2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 3-pyridine radicals 3-pyridine radicals 4-pyridine radicals 4-pyridine radicals 2-F-Ph H H H H H H H H H H H H H H H H H H H H H H H B5 B6 B7 B8 B9 B10 B11 B20 B24 B25 B26 B28 B30 B31 B32 B33 B43 B46 B7 B7 B7 B7 B7 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me H H H H H H H H H H H H H H H H H H Cl H Cl H Me H H H H H H H H H H H H H H H H H H Me H Me H Me
Table 6 (continuing)
R 1 R 2 B Y 1 Y 2 Y 3
2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 3-F-Ph 4-F-Ph 2，3-F 2-Ph 2，4-F 2-Ph 2，5-F 2-Ph Ph Ph Ph Ph H H H H H H H H H H H H H H H H H H H H H H H B7 B7 B7 B7 B7 B7 B1 B3 B6 B7 B3 B6 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 Me Cl Cl OMe SMe CF 3 Cl Cl Cl Cl CF 3 CF 3 CF 3 Cl Cl Cl CF 3 Cl Cl Me Me Cl Cl Cl Me H H H H Cl Cl Cl Cl Cl Cl Cl H Cl Cl Cl Cl Cl Me Cl Me H Me Me H H H Me Me Me Me Me Me Me Me H Me Me Me Me Me Me Me Me H
Table 6 (continuing)
R 1 R 2 B Y 1 Y 2 Y 3
Ph Ph Ph Ph Ph Ph Ph Ph Ph Ph Ph Ph 3，4-F 2-Ph 3，5-F 2-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph H H H H H H H H H H Me H H H H H H H H H H H H B7 B7 B7 B1 B3 B6 B7 B3 B6 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B6 B7 OMe SMe CF 3 Cl Cl Cl Cl CF 3 CF 3 CF 3 CF 3 Cl Cl Cl Me Me Cl Cl OMe SMe CF 3 Cl Cl H H H Cl Cl Cl Cl Cl Cl Cl Cl H Cl Cl Me Cl Me H H H H Cl Cl H H Me Me Me Me Me Me Me Me Me H Me Me Me Me Me H H H Me Me Me
Table 6 (continuing)
R 1 R 2 B Y 1 Y 2 Y 3
2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 3-Cl-Ph 4-Cl-Ph 2，3-Cl 2-Ph 2，4-Cl 2-Ph 2，5-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph H H H H H H H H H H H H H H H H H H H H Me H H B3 B6 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B1 B3 B6 B7 B7 B3 B6 CF 3 CF 3 CF 3 Cl Cl Cl Cl Cl Cl Me Me Cl Cl OMe SMe CF 3 Cl Cl Cl Cl Cl CF 3 CF 3 Cl Cl Cl H Cl Cl Cl Cl Cl Me Cl Me H H H H Cl Cl Cl Cl Cl Cl Cl Me Me Me H Me Me Me Me Me Me Me Me H H H Me Me Me Me Me Me Me Me
Table 6 (continuing)
R 1 R 2 B Y 1 Y 2 Y 3
2，6-Cl 2-Ph 2，6-Cl 2-Ph 3，4-Cl 2-Ph 3，5-Cl 2-Ph 2-Me-Ph 2-Me-Ph 2，6-Me 2-Ph 2，6-Me 2-Ph 2-MeO-Ph 2-MeO-Ph 2-CF 3O-Ph 2-CF 3O-Ph 2-SMe-Ph 2-SOMe-Ph 2-SO 2Me-Ph 2-CF 3-Ph 2-NO 2-Ph 2-NO 2-Ph 2-CN-Ph 2-NHMe-Ph 2-NMe 2-Ph 4-benzyl-Ph 4-phenoxy group-Ph H Me H H H H H H H H H H H H H H H H H H H H H B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B9 B7 B7 B7 B7 B7 CF 3 CF 3 Cl Cl Cl CF 3 Cl CF 3 Cl CF 3 Cl CF 3 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 6 (continuing)
R 1 R 2 B Y 1 Y 2 Y 3
4-tBu-Ph 2-OH-Ph 2-CO 2Me-Ph 2-CO 2Et-Ph H Me Et nPr iPr iPr nBu nBu iBu iBu iBu iBu iBu secBu secBu amyl group-2 2,2-Me2-propyl group nHex vinyl H H H H H H H H H H H H H H Me Me H H H H H H H B1 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B1 B7 B7 B7 Cl Cl Cl Cl Cl Cl Cl Cl Cl CF 3 Cl CF 3 Cl CF 3 Cl CF 3 Cl Cl CF 3 Cl Cl Cl Cl H Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl H Cl Cl Cl Cl Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me H Me Me Me Me Me Me
Table 6 (continuing)
R 1 R 2 B Y 1 Y 2 Y 3
1-propenyl 1-propenyl ethynyl 1-proyl CF 3 CHF 2 C 2F 5 2，2-Cl 2-cPr 2，2-Cl 2-cPr cPr cPr 1-Me-cPr 1-Me-cPr cHex cHex CH 2Ph naphthyl-1 naphthyl-1 naphthyl-2 naphthyl-2 CO 2Me CO 2Et 2-thienyl H H H H H H H H H H H H H H H H H H H H H H H B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B9 B7 B7 B7 B7 Cl CF 3 Cl Cl Cl Cl Cl Cl CF 3 Cl CF 3 Cl CF 3 Cl CF 3 Cl Cl CF 3 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl H Cl Cl Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me H Me Me Me Me
Table 6 (continuing)
R 1 R 2 B Y 1 Y 2 Y 3
2-thienyl CH 2OMe CH 2OEt COCH 3 COtBu COPh H H H H H H B7 B7 B7 B7 B7 B7 CF 3 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me Me Me Me Me
Table 7
Or
R 1 R 2 B Y 1 Y 2
Ph Ph Ph Ph Ph Ph Ph Ph Ph Ph Ph Ph Ph Ph Ph Ph tBu tBu tBu tBu tBu tBu tBu H H H Me H H H H H H H H H H H H H H H H H H H B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B4 B7 B9 B7 B7 B7 B7 B7 B7 B7 Me Me Et Et Me Cl Br Me Me CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Me Et Cl Cl Me Cl Br H Me Me Me Cl Me Me Br CF 3 H Br NO 2 CN Me Me Me Me Me Cl Me Cl CF 3 Me
Table 7 (continuing)
R 1 R 2 B Y 1 Y 2
TBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals H H H H H H H H H H H H H H H H H H H H H H H B7 B7 B7 B7 B7 B7 B7 B4 B5 B6 B7 B9 B20 B24 B25 B26 B7 B7 B7 B7 B7 B7 B7 Me Me CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Me Et Cl Cl Cl Me Br Br CF 3 Me H Br NO 2 CN Me Me Me Me Me Me Me Me Me Me Me Cl Me CF 3 Cl Me
Table 7 (continuing)
R 1 R 2 B Y 1 Y 2
2-thienyl 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 3-pyridine radicals 4-pyridine radicals 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 3-F-Ph 4-F-Ph 2,3-F2-Ph 2，4-F 2-Ph 2，5-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph H H H H H H H H H H H H H H H H H H H H H H H B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B4 B7 B9 B7 B7 B7 B7 B7 B7 B7 B7 B7 B4 Me CF 3 CF 3 CF 3 Et CF 3 Me Et CF 3 CF 3 CF 3 CF 3 CF 3 Et Et Et Et Et Me Et CF 3 CF 3 CF 3 CF 3 H Br Me Me Me Me Me Cl H Me Me Me Me Me Me Me Me Me Me Cl H Me
Table 7 (continuing)
R 1 R 2 B Y 1 Y 2
2，6-F 2-Ph 2，6-F 2-Ph 3，4-F 2-Ph 3，5-F 2-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 3-Cl-Ph 4-Cl-Ph 2，3-Cl 2-Ph 2，4-Cl 2-Ph 2，5-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph H H H H H H H H H H H H H H H H H H H H H H H B7 B9 B7 B7 B7 B7 B7 B7 B4 B7 B9 B7 B7 B7 B7 B7 B7 B7 B7 B7 B4 B7 B9 CF 3 CF 3 Et Et Me Et CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Me Et CF 3 CF 3 CF 3 CF 3 CF 3 Me Me Me Me Me Me Cl H Me Me Me Me Me Me Me Me Me Me Cl H Me Me Me
Table 7 (continuing)
R 1 R 2 B Y 1 Y 2
3，4-Cl 2-Ph 3，5-Cl 2-Ph 2-Me-Ph 2-Me-Ph 2，6-Me 2-Ph 2，6-Me 2-Ph 2-MeO-Ph 2-MeO-Ph 2-CF 3O-Ph 2-SMe-Ph 2-SOMe-Ph 2-SO 2Me-Ph 2-CF 3-Ph 2-NO 2-Ph 2-CN-Ph 2-NMe 2-Ph 4-benzyl-Ph 4-phenoxy group-Ph 2-OH-Ph 2-CO 2Me-Ph 2-CO 2Me-Ph 2-CO 2Et-Ph 2-CO 2Et-Ph H H H H H H H H H H H H H H H H H H H H H H H B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 CF 3 CF 3 Et CF 3 Et CF 3 Et CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Et CF 3 Et CF 3 Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 7 (continuing)
R 1 R 2 B Y 1 Y 2
H Me Et nPr iPr iPr nBu nBu iBu iBu secBu secBu 2，2-Me 2-propyl group nHex vinyl 1-acrylic 1-acrylic acetenyl 1-propinyl CF3 CHF 2 C 2F 5 2，2-Cl 2-cPr H H H H H H H H H H H H H H H H H H H H H H H B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 CF 3 CF 3 CF 3 CF 3 Et CF 3 Et CF 3 Et CF 3 Et CF 3 CF 3 CF 3 CF 3 Et CF 3 CF 3 CF 3 Et CF 3 CF 3 Et Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 7 (continuing)
R 1 R 2 B Y 1 Y 2
2，2-Cl 2-cPr cPr cPr 1-Me-cPr 1-Me-cPr cHex cHex CH 2Ph naphthyl-1 naphthyl-1 naphthyl-2 CO 2Me CO 2Et 2-thienyl H H H H H H H H H H H H H H B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 CF 3 Et CF 3 Et CF 3 Et CF 3 CF 3 Et CF 3 CF 3 CF 3 CF 3 CF 3 Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 8
Figure C9719404102311
Or
Figure C9719404102312
R 1 R 2 B W
2-F-Ph 2，6-F 2-Ph tBu tBu tBuCH 2 EtMe 2C cHex 1-Me-cHex Ph 2-F-Ph 2-Cl 2-Cl-Ph 2，6-F 2-Ph 2，6-Cl 2-Ph 1-naphthyl 2-naphthyl tBu tBu 2-pyridine radicals 3-pyridine radicals 4-pyridine radicals Me2C＝N- iPr H H H H H H H H H H H H H H Cl Me H H H H H H H H CO(2，4-Me 2-Ph) H B7 B6 B30 B31 B32 B33 B34 H CO 2iPr CO(2-MeO-Ph) H CO(4-MeO-Ph) CO(2-Me-Ph) Na Ca H H B7 B10 B13 2-F 2-F 2-F 2-F 2-F 2-F 2-Cl 2-Br 2-F 2-F 2-Me 2-nBu 2-OMe 2-nBeO 2-CF 3 2-OCHF 2 2-CF 3 2-OCH 2CH 2CHFCHF 2 2-OCF 2CHF 2 2-SMe 2-SOMe 2-SO 2Me 2-SCBrF 2
Table 8 (continuing)
R 1 R 2 B W
tBu tBuCH 2 EtMe 2C cHex Ph 2-F-Ph 2-F-Ph 2-CF 3-Ph 2，6-F 2-Ph 1-naphthyl PhCH 22-thienyl 4-Cl-2-thienyl 3-MeO-2-pyridyl 2-Cl-3-pyridyl 2,6-Cl 2-4-pyridyl EtMeC=N-Et tBu tBuCH 2 EtMe 2C cHex Ph H H H H H H H H H H H H H H H H H H H H H H H B19 B22 B23 B7 B25 B26 B27 B28 CO(2，6-Me 2-Ph) CO(2，6-(MeO) 2-Ph) CO(2-Me-6-NO 2-Ph) CO(3，4，5-(MeO) 3-Ph) SO 2(4-Me-Ph) CO(2，6-Cl 2-Ph) CO(2，5-Me 2-Ph) CO(2，6-F 2-Ph) B1 B2 B4 H H H H 2-SCF 3 2-SOCBrF 2 2-SO 2CH 2F 2-SCF 3 2-SCBrF 2 2-SO 2CHF 2 2-SCBrF 2 2-CH＝CCl 2 2-OCH 2CH＝CH 2 2-OCH 2CH＝CCl 2 2-OCH 2CH＝CHCl 2-SCH 2CH＝CHMe 2-SOCH 2CH＝CH 2 2-SO 2CHMeCH＝CH 2 2-SCH 2CMe＝CF 2 2-SOCH 2CF＝CF 2 2-SO 2CH 2CH＝CF 2 2-CCH 2-CCI 2-OCH 2CCH 2-OCH 2CCCl 2-SCH 2CCMe 2-SOCH 2CCH
Table 8 (continuing)
R 1 R 2 B W
2-MeO-Ph 2-F-Ph 2，6-F 2-Ph 2，6-Me 2-Ph 1-naphthyl PhCH 22-naphthyl 5-Br-3-thienyl 3-MeO-2-pyridyl 2-Cl-3-pyridyl 2,6-Cl 2-4-pyridyl (CH 2) 4C＝N- tBu tBuCH 2 EtMe 2C 2-Me-cHex Ph Ph 2-CF 3-Ph 2，6-F 2-Ph 2，6-Me 2-Ph 1-naphthyl PhCH 2 H H H H H H H H H H H H H H H H H H H H H H H B5 B6 B7 B8 Ba K H B3 B14 B15 B16 B17 H H H H B22 B27 B28 B30 B31 CO(3，4-(MeO) 2-Ph) CO(2，4-Cl 2-Ph) 2-SO 2CH 2CCMe 2-SCH 2CCBr 2-SOCHMeCCCl 2-SO 2CH 2CCI 2-NO 2 2-CN 2-CO 2Me 2-COMe 2-O(CO)Me 2-NHMe 2-NMe 2 3-F 3-Cl 3-nBu 3-OEt 3-CH 2CH 2CH 2CHF 2 3-OCH 2CH 2CHFCHF 2 3-S-nBu 3-SOnPr 3-SO 2iPr 3-SCF 3 3-SCH 2CH 2CHFCHF 2 3-SO 2CF 2CHF 2
Table 8 (continuing)
R 1 R 2 B W
2-thienyl 3-Me-2-pyridyl 3-NO 2-2-pyridyl 3,6-Cl 2-2-pyridyl 2-MeS-3-pyridyl (CH 2) 5C＝N- sBu tBuCH 2 EtMe 2C 2-Me-cHex Ph 2-CF 3O-Ph 2-MeS-Ph 2，6-F 2-Ph 2，6-Cl 2-Ph 1-naphthyl 3-F-2-pyridyl 6-Me-2-pyridyl 4-CF 3-3-pyridyl 3-NO 2-3-pyridyl 2，4-Me 2-3-pyridyl iBuMeC＝N- tBu H H H H H H H H H H H H H H H H H H H H H H H CO(3-CF 3-Ph) CO(2-Me 2N-Ph) COiPr CO 2iPr CO 2tBu CONHMe CONHEt B19 B18 SO 2(2-Me-Ph) H H H Na K Mg Ca Ba COCEtMe 2 CO(3-MeO-Ph) CO-2-naphtyl CO(4-EtO-3-MeO-Ph) CO(3-Cl-4-MeO-Ph) 3-SCH 2CMe＝CH 2 3-SOCH 2CH＝CH 2 3-SO 2CHMeCH＝CH 2 3-SCH 2CMe＝CF 2 3-SOCH 2CF＝CCl 2 3-SO 2CH 2CH＝CH 2Cl 3-OCH 2CCH 3-SCH 2CCMe 3-SOCH 2CCH 3-SO 2CH 2CCMe 3-NO 2 3-CN 3-CO 2Et 3-COnPr 3-O(CO)nPr 3-NHBu 3-NEt 2 4-F 4-Cl 4-Br 4-I 4-Me 4-tBu
Table 8 (continuing)
R 1 R 2 B W
TBu tBu Ph Ph 2-pyridyl sBu tBuCH 2 EtMe 2C 2-Me-cHex Ph 2-CF 3-Ph 2-NO 2-Ph 2，6-F 2-Ph 2-Cl-6-F-Ph 1-naphthyl 2-pyridyl 3-pyridyl PhCH 22-thienyl 3-thienyl iBuMeC=N-tBu tBu H H H H H H H H H H H H H H H H H H H H H H H CO(3-F-4-nBuO-Ph) CH 2CO 2Me CH(Me)CO 2Et CMe 2CO 2nPr CH 2CN CH 2CH 2CH 2CN CH 2CO 2iPr H H H H B3 B4 B5 B6 B7 B8 B12 B21 B28 CO(2-MeO-Ph) H H 4-OMe 4-CF 3 4-OCHF 2 4-SMe 4-SOMe 4-SO 2nBu 4-SCF 3 4-SOCBrF 2 4-SO 2CH 2F 4-OCH 2CH＝CH 2 4-OCH 2CH-CCl 2 4-OCH 2CCH 4-OCH 2CCCl 4-SCH 2CCMe 4-SO 2CH 2CCMe 4-NO 2 4-CN 4-CO 2nBu 4-COiBu 4-O(CO)nPr 4-NHnBu 2，3-Cl 2 2，4-Cl 2
Table 8 (continuing)
R 1 R 2 B W
TBu Ph Ph 2-pyridyl sBu tBuCH 2 EtMe 2C 2-Me-cHex Ph 2-Me-Ph 2-MeO-Ph 2，6-F 2-Ph 2，6-Cl 2-Ph 1-naphthyl 2-pyridyl PhCH 23-pyridyl 4-pyridyl 2-thienyl iBuMeC=N-tBu tBu tBu H H H H H H H H H H H H H H H H H H H H H H H H H H B7 B8 B12 B23 B26 B28 CONHiPr Ca Ba H H H CO(2，3-Me 2-Ph) CO(3，4-Me 2-Ph) CH 2CO 2Et CHMeCO 2Me CH 2CN H B7 B8 3，4-Cl 2 3，5-Cl 2 2，5-Cl 2 2，6-Cl 2 2，6-Cl 2 2，6-Cl 2 2，3-F 2 2，3-F 2 2，3-F 2 2，4-F 2 2，4-F 2 2，5-F 2 2，6-F 2 2，6-F 2 2，6-F 2 2，6-F 2 2，6-F 2 2，6-F 2 2，6-F 2 2，6-F 2 2，6-F 2 2，6-F 2 2，6-F 2
Table 8 (continuing)
R 1 R 2 B W
tBu tBu tBu tBu tBu tBu tBuCH 2 EtMe 2C cHex cHex cHex 1-Me-cHex Ph Ph Ph 2-F-Ph 3-F-Ph 4-F-Ph 2-Cl-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph H Me H H H H H H H H H H H H H H H H H H H Me H B28 B31 B34 CO(2-MeO-Ph) CO(2-Cl-Ph) CO(2，6-Me 2-Ph) CO(2，6-(MeO) 2-Ph) CO(3，4，5-(MeO) 3-Ph) B28 B30 B34 SO 2(4-Cl-Ph) H B5 B6 B14 B19 B23 B24 H Ca B7 B9 2，6-F 2 2，6-F 2 2，6-F 2 2，6-F 2 2，6-F 2 2，6-F 2 2，6-F 2 2，6-F 2 2，6-F 2 2，6-F 2 2，6-F 2 2，6-F 2 2，6-F 2 2，6-F 2 2，6-F 2 2，6-F 2 2，6-F 2 2，6-F 2 2，6-F 2 2，6-F 2 2，6-F 2 2，6-F 2 2，6-F 2
Table 8 (continuing)
R 1 R 2 B W
1-naphthyl 2-naphthyl 2-thienyl 3-thienyl 2-pyridine radicals 3-pyridine radicals 4-pyridine radicals nPr2C＝N- tBu tBu tBu tBu tBu tBuCH 2 EtMe 2C cHex cHex Ph Ph 2-F-Ph 3-F-Ph 2-Cl-Ph 2，6-F 2-Ph H H H H Cl H H H Et Br H H H H H H H H H H H H H B10 B16 B22 B24 H B7 B18 B31 H H SO 2(4-Me-Ph) COnHex CO(2-Cl-6-F-Ph) CO(3，5-Cl 2-4-MeO-Ph) CO(3-Br-4-Me-Ph) H B6 B7 B8 B34 CO 2tBu CHMeCO 2Me B31 2，6-F 2 2，6-F 2 2，6-F 2 2，6-F 2 3，4-F 2 3，5-F 2 2，5-(CF 3) 2 2，6-(CF 3) 2 3，5-(CF 3) 2 5-Br-2-Cl 3-Br-4-Me 2-Cl-4-F 2-Cl-6-F 2-Cl-6-F 2-Cl-6-F 2-Cl-6-F 2-Cl-6-F 2-Cl-6-F 2-Cl-6-F 2-Cl-6-F 2-Cl-6-F 2-Cl-6-F 3-Cl-4-F
Table 8 (continuing)
R 1 R 2 B W
2，6-F 2-Ph tBu 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 1-naphthyl 2-naphthyl 2-thienyl 3-thienyl 2-pyridine radicals 3-pyridine radicals 4-pyridine radicals nPr2C＝N- tBu tBu tBu tBuCH 2 EtMe 2C cHex cHex 1-Me-cHex Ph Ph H H H H Br H H H H H H H H H H H H H H H H H H K Ba CO(4-nBuO-Ph) CO(4-Et 2N-Ph) CO(3-Me 2N-Ph) CO(4-Et-Ph) CO(3-F-4-Me-Ph) CO(3-MeO-4-Me-Ph) CO(2，3，6-F 3-Ph) CO(2-MeO-5-NO 2-Ph) CO(3，5-Me 2-Ph) H H H B1 B2 B3 B4 B5 B6 B7 B8 B9 4-Cl-3-F 2-F-6-I 2-F-6-I 2-F-6-I 2-Cl-5-SMe 2-Cl-5-SCBrF 2 2-Cl-5-SCF 3 2-Cl-5-SOMe 2-Cl-5-SO 2Me 2-Cl-4-NO 2 2，4-(OMe) 2 2，6-(OMe) 2 2，6-(OMe) 2 2，3-Me 2 2，4-Me 2 2，5-Me 2 2，6-Me 2 2，6-Me 2 2，6-Me 2 3，4-Me 2 3，5-Me 2 2-F-4-Me 2-F-4-Me
Table 8 (continuing)
R 1 R 2 B W
Ph 2-F-Ph 2-F-Ph 3-F-Ph 4-F-Ph 2-Cl-Ph 2，6-F 2-Ph 2，6-F 2-Ph tBu cHex 1-naphthyl 2-F-Ph 2-pyridine radicals 3-pyridine radicals 4-pyridine radicals nPr2C＝N- tBu tBu tBu tBu tBu tBuCH 2 EtMe 2C H H H H H H H H H H H H H H H H H H H H H H H B10 B11 B12 B13 B14 CH 2CN CMe 2CO 2Et CONHMe SO 2(4-Cl-Ph) CO(2-MeO-Ph) CO(2-Me-Ph) CO(2-Cl-Ph) CO(2，3-(MeO) 2-Ph) CO(3，4-Me 2-Ph) CO(3-MeO-4-EtO-Ph) B15 B16 B17 B18 B19 B20 B21 B24 2-F-4-Me 3-F-4-Me 3-I-4-Me 2-OMe-4-SMe 3-OMe-4-NO 2 2-Me-4-NO 2 2-Me-6-NO 2 2，3，6-F 3 2，3，6-F 3 2，3，6-F 3 2，3，6-F 3 2，3，6-F 3 2，4，5-F 3 2，4，5-F 3 2，4，5-F 3 2，3，5-I 3 2，3，5-I 3 2，3，4-(OMe) 3 2，4，5-(OMe) 3 3，4，5-(OMe) 3 2，4，6-Me 3 2，3，4，5-F 4 2，3，4，5-F 4
Table 8 (continuing)
R 1 R 2 B W
cHex cHex cHex 1-Me-cHex Ph Ph Ph 2-F-Ph 3-F-Ph 4-F-Ph 2-Cl-Ph 2，6-F 2-Ph 2，6-F 2-Ph H H H H H H H H H H H H H B25 B27 B28 B29 B30 B31 B32 B33 B34 H H B27 Ca 2，3，4，5-F 4 2，3，5，6-F 4 2，3，5，6-F 4 2，3，5，6-F 4 2，3，5，6-F 4 2，3，4，5，6-F 5 2，3，4，5，6-F 5 2，3，4，5，6-F 5 2，3，5，6-F 4-4-Me 2，3，5，6-F 4-4-Me 2，3，5，6-F 4-4-Me 2，3，5，6-F 4-4-Me 2，3，5，6-F 4-4-Me
Table 9
Figure C9719404102431
R 1 B Y 1
Me Et iPr nBu sBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tPen nHex nHep nOct nNon nDec PhCH 2 Ph(Me)CH PhMe 2C H B1 B2 B3 B4 H B7 B8 B8 B7 B5 B7 B8 4-Cl-PhCO 2 B6 B7 B8 B9 B10 B11 B12 B13 B14 H Me Et nPr iBu nHex Me MeO MeS CF 3 CF 3 CClF 2 CF 3CF 2 CF 3CF 2CF 2 MeO EtO iPrO sBuO MeS EtS nPrS tBuS Ph
Table 9 (continuing)
R 1 B Y 1
PhMe 2C PhMe 2C PhMe 2C PhMe 2C PhMe 2C PhMe 2C PhMe 2C PhMe 2C 4-Cl-PhMe 2C 3-Br-PhEtMeC 4-Me-Ph(CH 2) 3 CH 2＝CMe CF 3CF 2CF 2 cPr cPen cPen cPen cHex cHex cHex cHex cHex cHex B7 B8 B33 B34 B41 B7 B8 B34 B15 B16 B17 B18 B19 B20 B21 B22 B23 B24 B7 B8 B33 B34 B7 Me Me Me Me Me CF 3 CF 3 CF 3 Me 2N Et 2N H Me Et nPr iBu nHex CF 3 CClF 2 CF 3 CF 3 CF 3 CF 3 Me
Table 9:(is continuous)
R 1 B Y 1
cHex cHex 1-Me-cHex 1-Me-cHex 1-Me-cHex 1-Me-cHex 1-Me-cHex 1-Me-cHex EtO iPrO CF 3O tBuOC(O) Ph 2-F-Ph 2-F-Ph 2-Cl-Ph 2-Cl-Ph 2-Br-Ph 2-I-Ph 2-CF 3-Ph 2-MeO-Ph 3，4-Cl 2-Ph 2，4-Me 2-Ph B8 B34 B7 B8 B7 iBuOC(O) B28 B29 B30 B31 B32 B33 B34 B35 B36 B37 B38 B39 B40 B41 B42 CClF 2C(O) PhSC(O) Me Me Me CF 3 CF 3 CF 3 EtO iPrO sBuO MeS EtS nPrS tBuS Ph Me 2N Et 2N Cl Br I H CF 3 MeO MeS
Table 9 (continuing)
R 1 B Y 1
2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-thienyl 1-naphthyl 2-naphthyl tBu tBu B7 B7 B8 B8 EtSC (O) tBuC (S) cPenOC (O) cHexOC (O) B7 B8 B7 B8 iBuOC (O) B33 B34 B34 2-pyridine radicals-C (O) 2-pyridine radicals-C (O) 3-pyridine radicals-C (O) 4-pyridine radicals-C (O) H CClF2C(O) PhSC(O) Me CF 3 Me CF 3 H Me Et nPr Me Me CF 3 CF 3 CF 3 CF 3 CF 3 Me CClF 2 CF 3CF 2 CF 3CF 2CF 2 MeO EtO H Me
Table 9 (continuing)
R 1 B Y 1
tBu tBu cPr cPen cHex 1-Et-cPr 1-Me-cPen 1-Me-cPen 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph EtSC (O) tBuC (S) cPenOC (O) cHexOC (O) B7 B8 iBuOC (O) 2-pyridine radicals-C (O) 2-pyridine radicals-C (O) 2-pyridine radicals-C (O) 4-pyridine radicals-C (O) 2-pyridine radicals-C (O) Et nPr iBu nHex CF 3 CClF 2 CF 3CF 2 CF 3CF 2CF 2 MeO MeO Me CF 3
Table 10
Or
Figure C9719404102503
R 1 B A R 1 B A
Et iPr iBu sBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu H B7 B7 B7 B7 B8 B15 B34 B7 B8 B15 B34 CO 2-iBu B7 B7 B7 B7 H B7 B8 B15 B34 H A1 A2 A1 A2 A1 A1 A1 A1 A2 A2 A2 A2 A2 A3 A4 A5 A6 A7 A7 A7 A7 A7 A8 tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu B15 B34 H B7 B8 B15 B34 CO 2-iBu H B7 B8 B15 B34 CO 2-iBu H B7 B8 B15 H B7 B8 B15 B34 A8 A8 A9 A9 A9 A9 A9 A9 A10 A10 A10 A10 A10 A10 A11 A11 A11 A11 A12 A12 A12 A12 A12
Table 10 (continuing)
R 1 B A R 1 B A
tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu B7 B8 B7 B8 B15 B34 CO 2-iBu H B7 B16 B17 B7 B8 B9 B10 B11 B12 B13 B7 B8 B7 B8 B15 A8 A8 A13 A13 A13 A13 A13 A14 A14 A14 A14 A15 A16 A17 A18 A19 A20 A21 A22 A22 A23 A23 A23 tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBuCH 2 tBuCH 2 tBuCH 2 Et(Me) 2C CO 2-iBu H B17 B18 B19 B7 B8 B15 B20 H B7 B8 B15 B34 CO 2-iBu B21 B22 B23 B24 B3 B7 B8 B15 A12 A13 A27 A28 A29 A30 A30 A30 A31 A32 A32 A32 A32 A32 A32 A33 A34 A35 A36 A1 A2 A2 A2
Table 10 (continuing)
R 1 B A R 1 B A
tBu tBu tBu tBu nHex nHep nOct nNon nDec cPr 1-Me-cPr 1-Me-cPr 1-Me-cPr 1-Me-cPr 1-Me-cPr cPen cHex cHex cHex cHex cHex cHex cHex B34 B14 B15 B16 B7 B7 B7 B7 B7 B7 B7 B7 B8 B34 H B7 B7 B7 B8 B15 B34 B35 B36 A23 A24 A25 A26 A1 A2 A1 A2 A7 A8 A1 A2 A2 A2 A2 A2 A1 A2 A2 A2 A2 A2 A1 Et(Me) 2C Et(Me) 2C Et(Me) 2C Et(Me) 2C Ph Ph Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-F-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph B16 B34 H B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B8 B7 B7 B7 B7 B7 B7 B7 B8 A2 A2 A2 A2 A10 A13 A32 A1 A2 A7 A8 A9 A10 A13 A32 A1 A2 A7 A8 A9 A10 A13 A30
Table 10 (continuing)
R 1 B A R 1 B A
cHex Ph Ph Ph Ph Ph 2-Me-Ph 2-Me-Ph 2-MeO-Ph 2-CF 3-Ph 2-NO 2-Ph 2-CN-Ph 2-CBrF 2O-Ph 2-CF 3O-Ph 2-MeS-Ph 2-nBuS-Ph 2-MeSO-Ph 2-MeSO 2-Ph 2-CH 2＝CHCH 2S-Ph 2-CH 2＝CHCH 2SO-Ph 2-CH 2＝CHCH 2SO 2-Ph 2-CF 3S-Ph 2-CHF 2S-Ph B37 H B7 B7 B7 B7 B7 B7 B2 B3 B4 B5 B6 B7 B8 B9 B10 B11 B12 B13 B14 B15 B16 A2 A2 A2 A7 A8 A9 A1 A2 A7 A8 A9 A10 A11 A12 A13 A14 A15 A16 A17 A18 A19 A20 A21 2-Cl-Ph 2-Br-Ph 2-I-Ph 2-Me-Ph 2-Me-Ph 2-Me-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph B34 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B7 B3 B4 B5 B8 B15 A32 A1 A2 A7 A8 A9 A1 A2 A7 A1 A2 A7 A8 A9 A10 A13 A21 A32 A2 A2 A2 A2 A2
Table 10 (continuing)
R 1 B A R 1 B A
2-CBrF 2SO-Ph 2-CF 3SO 2-Ph 2-CHO-Ph 2-OH-Ph 2-Me 2N-Ph 3-Ph-Ph 4-PhO-Ph 2-MeOC(O)-Ph Cl PhCH 2 PhCH 2 PhCH 2 PhCH 2 (4-Cl-Ph)CH 2 (4-Me-Ph)CH 2 (3，4-Cl 2-Ph)CH 2 (2，4-Me 2-Ph)CH 2 PhMeCH Ph(Me) 2C Ph(Me) 2C Ph(Me) 2C Ph(Me) 2C Ph(Me) 2C B17 B18 B19 B20 B21 B22 B23 B24 B7 B7 B7 B8 B34 B7 B7 B7 B7 B7 B3 B7 B3 B7 B8 A22 A23 A24 A25 A26 A27 A28 A29 A1 A1 A2 A2 A2 A30 A31 A32 A33 A34 A1 A1 A2 A2 A2 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph ClCC 2，2-Cl 2-cPr 2，2-F 2-cBu MeO nHexO CH 2＝CHCH 2O CHCCH 2O CF 3O ClCH＝CHCH 2O MeS MeSO MeSO 2 Me 2C＝CHCH 2S Me 2C＝CHCH 2SO Me 2C＝CHCH 2SO 2 B19 B32 B33 B34 B35 B37 B40 B43 B3 B4 B5 B6 B7 B8 B9 B10 B11 B12 B13 B14 B15 B16 B17 A2 A2 A2 A2 A2 A2 A2 A2 A23 A23 A23 A24 A25 A26 A27 A28 A29 A30 A30 A30 A31 A32 A32
Table 10 (continuing)
R 1 B A R 1 B A
Ph(Me) 2C Ph(Me) 2C Ph(Me) 2C Ph(Me) 2C Ph(Me) 2C Ph(Me) 2C CF 3 CF 3CH 2 CH 2＝CMe Cl 2C＝CH BrCCCH 2SO ClCCH 2SO 21-naphthyl 2-naphthyl MeC (O) MeC (O) O CF 3C (O) O 2-thienyl 3-thienyl Me 2C＝N EtMeC＝N PhCH＝N PhMeC＝N B33 B34 B35 B7 B8 B34 B15 B6 B6 B29 B28 B29 B30 B31 B32 B33 B34 B35 B36 B37 B38 B39 B40 A2 A2 A2 A13 A13 A13 A35 A36 A1 A2 A1 A2 A2 A13 A13 A1 A1 A2 A2 A1 A1 A2 A2 CHCCH 2S CHCCH 2SO CHCCH 2SO 2 CF 3S CF 3SO CF 3SO 2 ClCH＝CHCH 2S ClCH＝CHCH 2SO ClCH＝CHCH 2SO 2 ClCCCH 2S 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals B18 B19 B20 B21 B22 B23 B24 B25 B26 B27 H B7 B8 B15 B34 H B7 B8 B15 B34 H B7 B8 A32 A1 A2 A2 A13 A13 A1 A1 A2 A2 A7 A7 A7 A7 A7 A8 A8 A8 A8 A8 A9 A9 A9
Table 10 (continuing)
R 1 B A R 1 B A
2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals B7 B8 B15 B34 B7 B8 B15 B34 CO 2-iBu B7 B7 B7 B7 H B7 B8 B15 B34 CO 2-iBu H B7 B8 B15 A1 A1 A1 A1 A2 A2 A2 A2 A2 A3 A4 A5 A6 A12 A12 A12 A12 A12 A12 A13 A13 A13 A13 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals B15 B34 CO 2-iBu H B7 B8 B15 B34 CO 2-iBu H B7 B8 B15 B8 B15 B34 B14 B15 B16 B17 B18 B19 B7 A9 A9 A9 A10 A10 A10 A10 A10 A10 A11 A11 A11 A11 A23 A23 A23 A24 A25 A26 A27 A28 A29 A30
Table 10 (continuing)
R 1 B A R 1 B A
2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals B34 CO 2-iBu H B7 B16 B17 B7 B8 B9 B10 B11 B12 B13 B7 B8 A13 A13 A14 A14 A14 A14 A15 A16 A17 A18 A19 A20 A21 A22 A22 2-pyridyl 2-pyridyl 2-pyridyl 2-pyridyl 2-pyridyl 2-pyridyl 3-pyridyl 3-pyridyl 3-pyridyl 3-pyridyl 3-pyridyl 4-pyridyl 4-pyridyl 4-pyridyl 4-pyridyl B8 B15 B20 H B7 B8 B7 B34 CO 2-iBu B7 B8 B7 B8 B15 B34 A30 A30 A31 A32 A32 A32 A1 A2 A2 A13 A13 A1 A1 A2 A2
Table 11
Figure C9719404102591
Or
Figure C9719404102592
G B Y 1 Y 2 Y 3
2-Cl 3-Cl 4-Cl 4-Br 4-I 4-F 4-Me 4-Et 4-iPr 4-nBu 4-iBu 4-sBu 4-sBu 4-sBu 4-sBu 4-sBu 4-sBu 4-sBu 4-sBu 4-sBu 4-sBu 4-sBu 4-sBu H B1 B2 B3 B4 B5 B6 B7 B8 B9 B10 B11 H B16 B17 B7 B8 B16 B17 B34 B3 B7 B8 Me Me Cl Cl CF 3 CF 3 H H Cl H OMe SMe Me Me Me Me Me Me Me Me CF 3 CF 3 CF 3 Me Cl Me Cl Cl H CF 3 Cl H H Cl Cl Me Me Me Cl Cl Cl Cl Cl Cl Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 11 (continuing)
G B Y 1 Y 2 Y 3
4-sBu 4-sBu 4-sBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu B34 B7 B17 B12 H B3 B7 B8 B15 B16 B28 B30 B34 CO-nC 8H 17 CO-nC 15H 31 CO 2-nHex CO 2-nC 10H 21 H H B3 B7 B8 B15 CF 3 Cl Cl SCF 3 Me Me Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl CN CF 3 CF 3 CF 3 CF 3 CF 3 Cl Cl Cl Cl Me Cl Me Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 11 (continuing)
G B Y 1 Y 2 Y 3
4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBuCH 2 4-tBuCH 2 4-tBuCH 2 4-tBuCH 2 4-tBuCH 2 4-tBuCH 2 4-Et(Me) 2C B16 B28 B30 B16 B16 B17 B17 CO 2-nC 10H 21 CH 2OEt B7 B7 B7 B16 B3 2-(4-tBu-Ph)-3，3-Me 2-cPrC(O) B45 B3 B7 B16 B7 B8 B7 H CF 3 CF 3 CF 3 Cl CF 3 CF 3 Cl CF 3 CF 3 Me Me CN CN CN CF 3 CF 3 CF 3 Me Me CF 3 CF 3 Cl CF 3 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Cl Cl Cl Cl Cl Cl Me Cl Cl Cl Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 11 (continuing)
G B Y 1 Y 2 Y 3
4-Et(Me) 2C 4-Et(Me) 2C 4-Et(Me) 2C 4-Et(Me) 2C 4-Et(Me) 2C 4-Et(Me) 2C 4-Et(Me) 2C 4-Et(Me) 2C 4-Et(Me) 2C 4-Et(Me) 2C 4-Et(Me) 2C 4-Et(Me) 2C 4-Et(Me) 2C 4-Et(Me) 2C 4-Et(Me) 2C 4-Et(Me) 2C 4-Et(Me) 2C 4-Et(Me) 2C 4-Et(Me) 2C 4-nHex 4-nHep 4-nOct 4-nNon B3 B7 B8 B34 B42 B16 B17 H B7 B8 B7 B7 B4 B5 B6 B3 B16 B17 B24 B34 B42 B43 B43 CF 3 CF 3 CF 3 CF 3 CF 3 Me Me Cl Cl Cl CF 3 CN H Cl H Cl Cl Cl Cl CF 3 CF 3 Me Me Cl Cl Cl Cl Cl Me Me Me Cl Cl Me Cl Cl H H Cl Cl Cl Cl Cl Cl Me Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 11 (continuing)
G B Y 1 Y 2 Y 3
4-nDec 4-(Me) 2(CN)C 4-PhCH 2 4-Ph(Me) 2C 4-(4-F-Ph)(Me) 2C 4-MeCH＝CH 4-MeCC 3-CF 3 4-CF 3 4-CF 3 4-CF 3 4-CF 3 4-CF 3 4-CF 3 4-CF 3 4-CF 3 4-CF 3 4-CF 3 4-CF 3 4-CF 3CH 2 4-Cl 2C＝CHCH 2 4-BrCC 4-(2，2-F 2)cBuCH 2 H B7 B7 B7 B7 B4 B5 B6 B7 B8 B9 B16 B17 B16 B17 B7 B7 B7 B3 B7 B8 B7 B7 Cl Cl CF 3 CF 3 CN H Cl H OMe SMe SCF 3 Me Me Me Cl Cl CF 3 CN Cl Me Cl Cl CF 3 Me Cl Cl Me Cl Cl H H Cl Cl Cl Me Me Cl Me Cl Cl Cl Cl Cl Me Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 11 (continuing)
G B Y 1 Y 2 Y 3
4-(1-Me)cPr 4-cHex 4-(1-Me)cHex 4-MeO 4-iPrO 4-iPrO 4-iPrO 4-iPrO 4-iPrO 4-iPrO 4-iPrO 4-tBuO 4-tBuO 4-tBuO 4-nHexO 4-nOctO 4-nDecO 4-CH 2＝CHCH 2O 4-CHCCH 2O 4-CHF 2O 4-CHF 2O 4-CHF 2O 4-CHF 2O B16 B7 B8 B7 B7 B7 B15 B7 B16 B17 B23 B7 B8 B7 B8 B34 H B7 B8 B34 B7 B35 B36 CN Cl CF 3 Cl Cl CF 3 CF 3 Me Me Me SCF 3 Cl Cl CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Me Me Cl Cl Cl Cl H Cl Cl Cl Me Me Me Cl Cl Cl Cl Cl Cl Cl Cl Cl 3 Cl Me Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 11 (continuing)
G B Y 1 Y 2 Y 3
4-CHF 2O 4-CBrF 2O 4-CBrF 2O 4-CBrF 2O 4-CBrF 2O 4-CBrF 2O 4-CBrF 2O 4-CBrF 2O 4-CBrF 2O 4-CBrF 2O 4-CBrF 2O 4-CF 3O 4-CF 3O 4-CF 3O 4-CF 3O 4-CF 3O 4-CF 3O 4-CF 3CH 2O 4-CF 2＝CHCH 2CH 2O 4-CCl 2＝CHCH 2O 4-ClCCCH 2O 4-MeS 4-sBuS B7 B8 B34 B40 B41 B42 B43 B44 COCO 2Me H B1 B2 B3 B4 B5 B6 B7 B8 B9 B10 B11 B12 H Cl Cl Cl Me Me Cl Cl CF 3 CF 3 H H Cl H OMe SMe SCF 3 Me Me Me Cl Cl CF 3 CF 3 Cl Cl Cl Me Cl Me Cl Cl H CF 3 Cl H H Cl Cl Cl Me Me Cl Me Cl Cl H Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 11 (continuing)
G B Y 1 Y 2 Y 3
4-EtSO 4-MeSO 2 4-MeSO 2 4-MeSO 2 4-MeSO 2 4-EtSO 2 4-EtSO 2 4-iPrSO 2 4-iPrSO 2 4-tBuSO 2 4-tBuSO 2 4-MeCH＝CHCH 2S 4-CH 2＝CHCH 2SO 4-CH 2＝CHCH 2SO 2 4-CHCCH 2S 4-CHCCH 2SO 4-CHCCH 2SO 2 4-CHF 2S 4-CHF 2S 4-CHF 2S 4-CHF 2S 4-CHF 2S 4-CHF 2S B3 H B3 B32 B33 H B3 B32 B33 B7 B33 B15 B16 B28 B30 B34 CO-nC 8H 17 H B7 B8 B15 B29 H H CF 3 CF 3 CF 3 CF 3 CF 3 Cl Cl Cl Cl CF 3 H OMe SMe SCF 3 Me Me CF 3 CF 3 CF 3 CF 3 CF 3 Cl CF 3 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl H Cl Cl Cl Me Me Cl Cl Cl Cl Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 11 (continuing)
G B Y 1 Y 2 Y 3
4-CHF 2S 4-CHF 2S 4-CBrF 2S 4-CBrF 2S 4-CBrF 2S 4-CBrF 2S 4-CBrF 2S 4-CBrF 2S 4-CBrF 2S 4-CBrF 2S 4-CBrF 2S 4-CBrF 2S 4-CBrF 2S 4-CBrF 2S 4-CBrF 2S 4-CF 3S 4-CF 3S 4-CF 3S 4-CF 3S 4-CF 3S 4-CF 3S 4-CF 3S 4-CF 3S B7 B15 B7 B15 B30 B43 CO-nC 15H 31 CO 2-nHex H B7 B8 B15 B28 B34 B7 CO 2-nC 10H 21 H B3 B7 B8 B15 H B7 Cl Cl Cl Cl Cl Cl Me CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Me Cl Cl Cl Cl Cl Cl CF 3 CF 3 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 11 (continuing)
G B Y 1 Y 2 Y 3
4-CF 3S 4-CF 3S 4-CF 3S 4-CF 3S 4-CF 3S 4-CF 3S 4-CF 3S 4-CF 3CH 2S 4-CHF 2CF 2S 4-CHF 2SO 4-CBrF 2SO 4-CBrF 2SO 4-CBrF 2SO 4-CBrF 2SO 4-CBrF 2SO 4-CBrF 2SO 4-CF 3SO 4-CF 3SO 4-CF 3SO 4-CF 3SO 4-CF 3CH 2SO 2 4-CHF 2CF 2SO 2 4-CHF 2SO 2 B8 B15 B34 CO 2-nC 12H 25 CO-nC 15H 31 CO-nC 16H 33 CO-nC 17H 35 CO-nC 18H 37 CO-nC 19H 39 CO-nC 20H 41 H B3 B7 B24 B32 B33 H B3 B7 B33 B15 B16 B28 CF 3 CF 3 CF 3 CF 3 CF 3 Me Me CF 3 CF 3 H H CF 3 CF 3 CF 3 CF 3 CF 3 Cl Cl Cl Cl H OMe SMe Cl Cl Cl Cl Cl Me Cl Cl H CF 3 Cl Cl Cl Cl Cl Cl Cl Cl Cl H H Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 11 (continuing)
G B Y 1 Y 2 Y 3
4-CHF 2SO 2 4-CHF 2SO 2 4-CHF 2SO 2 4-CHF 2SO 2 4-CHF 2SO 2 4-CHF 2SO 2 4-CHF 2SO 2 4-CHF 2SO 2 4-CBrF 2SO 2 4-CBrF 2SO 2 4-CBrF 2SO 2 4-CBrF 2SO 2 4-CBrF 2SO 2 4-CBrF 2SO 2 4-CBrF 2SO 2 4-CBrF 2SO 2 4-CBrF 2SO 2 4-CBrF 2SO 2 4-CBrF 2SO 2 4-CBrF 2SO 2 4-CBrF 2SO 2 4-CBrF 2SO 2 4-CBrF 2SO 2 B7 B24 B32 B33 H B3 B7 B33 H B2 B3 B18 B19 B33 H B3 B7 B20 B32 B33 B37 B7 B15 CF 3 CF 3 CF 3 CF 3 Cl Cl Cl Cl SCF 3 Cl Cl Cl Cl Cl CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Me Me Cl Cl Cl Cl Cl Cl Cl H Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 11 (continuing)
G B Y 1 Y 2 Y 3
4-CBrF 2SO 2 4-CBrF 2SO 2 4-CBrF 2SO 2 4-CF 3SO 2 4-CF 3SO 2 4-CF 3SO 2 4-CF 3SO 2 4-CF 3SO 2 4-CF 3SO 2 4-CF 3SO 2 4-CF 3SO 2 4-Cl 2C＝CHCH 2S 4-Cl 2C＝CHCH 2SO 4-Cl 2C＝CHCH 2SO 2 4-CBrCCH 2S 4-CBrCCH 2SO 4-CBrCCH 2SO 2 4-CHO 4-NO 2 4-CN 4-(Me) 2N 4-Me(MeCO)N 4-PhMeN B17 B7 B16 B16 B7 B15 B3 B7 B15 B7 B8 B16 B17 B17 CO 2-nC 10H 21 B33 B7 B7 B8 B16 B3 B7 B8 Me Me Me Me Cl Cl CF 3 CF 3 Me Me Me Me Me Cl Cl CF 3 CF 3 H H Cl H OMe SMe Me Cl Cl Me Cl Cl Cl Cl Me Cl Cl Me Cl Me Cl Cl H CF 3 Cl H H Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 11 (continuing)
G B Y 1 Y 2 Y 3
4-PhCH 2(MeCO) N 4-(1-naphthyl) 4-(2-naphthyl) 4-(2-Cl-Ph) CH 2O 4-(3-Cl-Ph)CH 2O 4-(4-Cl-Ph)CH 2O 4-(4-Cl-Ph)CH 2O 4-(4-Cl-Ph)CH 2O 4-(4-F-Ph)CH 2O 4-(2-Me-Ph)CH 2O 4-(4-Me-Ph)CH 2O 4-(4-Et-Ph)CH 2O 3-(2，4-Cl 2-Ph)CH 2O 4-(3，4-Cl 2-Ph)CH 2O 4-(2，5-Me 2-Ph)CH 2O 4-(2，3，4，5，6-F 5-Ph)CH 2O 4-MeOC(O) 4-EtOC(O) 4-nPrOC(O) 4-iPrOC(O) 4-iBuOC(O) 4-tBuOC(O) 4-tBuCH 2OC(O) B15 B16 B28 B30 B34 B7 B7 B37 B42 B43 B43 H B7 B7 B7 B7 B4 B5 B6 B7 B8 B9 B7 SCF 3 Me Me Me Cl CF 3 Cl Cl CF 3 CF 3 H H Cl H OMe SMe SCF 3 Me Me Me Cl Cl Cl Cl Me Me Cl Me Cl Cl Cl Cl H CF 3 Cl H H Cl Cl Cl Me Me Cl Me Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 11 (continuing)
G B Y 1 Y 2 Y 3
4-tBuCH 2OC(O) 4-tBuCH 2OC(O) 4-tBuCH 2OC(O) 4-tBuCH 2OC(O) 4-tBuCH 2OC(O) 4-tBuCH 2OC(O) 4-Et(Me) 2COC(O) 4-nHexOC(O) 4-MeOCH 2 4-EtOCH 2 4-iPrOCH 2 4-MeC(O) 4-EtC(O) 4-iPrC(O) 4-tBuC(O) 4-tBuC(O) 4-tBuC(O) 4-tBuC(O) 4-tBuC(O) 4-tBuC(O) 4-tBuC(O) 4-tBuC(O) 4-tBuC(O) B15 B34 B7 B15 B34 B10 B11 B7 B8 B7 B7 B16 B7 B8 H B3 B7 B3 B7 B15 B7 B17 B16 Cl Cl CF 3 CF 3 CF 3 CF 3 CF 3 H H Cl H OMe SMe SCF 3 Cl Cl Cl CF 3 CF 3 CF 3 Me Me Me Cl Cl Cl Cl Cl Cl H CF 3 Cl H H Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 11 (continuing)
G B Y 1 Y 2 Y 3
4-CF 3C(O) 4-CF 3CF 2C(O) 4-CF 2CF 2CF 2C(O) 4-MeC(O)O 4-iPrC(O)O 4-tBuC(O)O 4-CF 3C(O)O 4-CF 2CF 2CF 2C(O)O 4-Me 2NC(O)O 4-Et 2NC(O)O 4-(nPr) 2NC(O)O 3-Ph 4-Ph 4-(4-F-Ph) 4-(4-F-Ph) 3-PhO 3-PhO 4-PhO 4-(4-F-Ph)O 4-(4-Cl-Ph)O 4-(4-Br-Ph)O 4-(4-Me-Ph) 4-(2-Cl-Ph)O B7 B8 B22 B23 B7 B8 B7 B8 B34 H B7 B8 B34 B7 B7 B7 B15 B7 B35 B36 B7 B8 B34 Me Me Cl Cl CF 3 CF 3 H H Cl H OMe SMe SCF 3 Cl CF 3 Cl CF 3 Me Me Cl Cl CF 3 CF 3 Me Cl Me Cl Cl H CF 3 Cl H H Cl Cl Cl Cl Cl Cl Cl Me Cl Me Cl Cl H Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 11 (continuing)
G B Y 1 Y 2 Y 3
4-(2-F-Ph)O 4-(3-Cl-Ph)O 4-(4-Cl-Ph)O 4-(2，4-Cl 2-Ph)O 4-(3，4-Cl 2-Ph)O 4-(3，4，5-Cl 3-Ph)O 4-(2-Me-Ph)O 4-(4-Me-Ph)O 4-(3-Cl-4-Me-Ph)O 4-(2-pyridyl) 4-(5-CF 3-pyridine radicals-2-yl) 4-(2-pyridine radicals) O 4-(2-pyridine radicals) O 4-(2-pyridine radicals) O 4-(2-pyridine radicals) O 4-(2-pyridine radicals) O 4-(2-pyridine radicals) O 4-(5-CF3-pyridyl-2-yl) O 4-(5-CF 3-pyridyl-2-yl) O 4-(5-CF 3-pyridyl-2-yl) O 4-(5-CF 3-pyridyl-2-yl) O 4-(5-CF 3-pyridyl-2-yl) O 4-(5-CF 3-pyridyl-2-yl) O B40 B41 B42 B43 B44 COCO 2Me H B1 B2 B3 B4 B7 B15 B7 B8 B34 B5 B7 B8 B15 B7 B15 B34 H H Cl H OMe SMe SCF 3 Me H H Cl Cl Cl CF 3 CF 3 CF 3 Cl Cl Cl CF 3 CF 3 CF 3 Me CF 3 Cl H H Cl Cl Cl Me CF 3 Cl H Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 11 (continuing)
G B Y 1 Y 2 Y 3
4-(3-Cl-5-CF 3-pyridyl-2-yl) 4-(3-Cl-5-CF 3-thiophene-2-yl) 4-(3-Cl-5-CF 3-pyridyl-2-yl) 4-(3-Cl-5-CF 3-pyridyl-2-yl) 4-(3-Cl-5-CF 3-pyridyl-2-yl) 4-(3-Cl-5-CF 3-pyridyl-2-yl) 4-(3-Cl-5-CF 3-pyridyl-2-yl) 4-(5-Cl-thiophene-2-yl) 3-OCH 2O-4 4-OCF 2O-4 4-MeCH＝N 4-Me 2C＝N 4-MeEtC＝N 4-PhCH＝N 4-PhMeC＝N 4-PhCH 2CH＝N 4-cC 6H 10＝N 3-CH 2CH 2CH 2-4 3-CH 2CH 2CH 2CH 2-4 4-PhC(O) 4-PhC(O) 4-PhC(O) 4-PhC(O) B7 B15 B34 B7 B15 B17 H B8 B9 B10 B11 B12 H B3 B7 B8 B15 B16 B28 H B7 B7 B33 Cl Cl Cl CF 3 CF 3 CF 3 Cl Cl Cl CF 3 CF 3 CF 3 Cl Cl Cl CF 3 CF 3 CF 3 Cl Cl Cl Cl CF 3 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 11 (continuing)
G B Y 1 Y 2 Y 3
4-(2-Cl-Ph)C(O) 4-(4-F-Ph)C(O) 4-(4-Cl-Ph)C(O) 4-(4-Cl-Ph)C(O) 4-(4-Cl-Ph)C(O) 4-(4-Me-Ph)C(O) 4-(4-Me-Ph)C(O) 4-(3，4-Cl 2-Ph)C(O) 3，4-Cl 2 3-Cl-4-F 2，6-F 2 3-Cl-4-CF 3 4-tBu-3-Cl 4-tBu-3-Cl 4-tBuCH 2-3-Cl 4-nHep-3-Cl 3-Cl-4-iPrO 3-Cl-4-iPrO 3-Cl-4-nHepO 3-Cl-4-(3，4-Cl 2-PhCH 2)O 3-Cl-4-PhCH 2O 3，4-(MeO) 2 4-MeO-3-Me B7 H B7 B15 B34 B3 B16 B45 B15 B7 B15 B7 B7 B15 B7 B15 B7 B7 B15 H B7 B16 B17 CF 3 CF 3 Cl Cl Cl CF 3 CF 3 CF 3 Cl Cl CF 3 CF 3 Cl CF 3 Cl CF 3 Cl CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 11 (continuing)
G B Y 1 Y 2 Y 3
4-OH-3，5-(tBu) 2 3，4，5-Cl 3 2，6-Cl 2-4-CF 3 2，6-F 2-4-CF 3 2，6-F 2-4-CF 3O 3，5-Cl 2-4-tBu 3，5-Cl 2-4-tBuCH 2 3，5-Cl 2-4-nDec 3，5-Cl 2-4-PhCH 2O 2，3，5，6-F 4-4-Me 2，3，4，5，6-F 5 B3 B15 B7 B15 B7 B7 B15 B7 B15 B3 B33 CF 3 CF 3 CF 3 Cl CF 3 Cl CF 3 Cl CF 3 CF 3 CF 3 Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Cl Me Me Me Me Me Me Me Me Me Me Me
Table 12
Or
Figure C9719404102792
G B Y 1 Y 2
2-Cl 3-Cl 4-Cl 4-Br 4-I 4-F 4-Me 4-Et 4-iPr 4-nBu 4-iBu 4-sBu 4-sBu 4-sBu 4-sBu 4-sBu 4-sBu 4-sBu 4-sBu 4-sBu 4-sBu 4-sBu 4-sBu H B1 B2 B3 B4 B5 B6 B7 B8 B9 B10 B11 H B16 B17 B7 B8 B16 B17 B34 B3 B7 B8 Me H Me H Me CF 3 Cl H Cl H OMe SMe Me Et Cl Cl CF 3 Me Me CF 3 CF 3 CF 3 Cl Me H H Me Me Me Me Me Me Me Me Me Me Me Me Cl Me CF 3 Me Me Me Me Me
Table 12 (continuing)
G B Y 1 Y 2
4-sBu 4-sBu 4-sBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu B34 B7 B17 B12 H B3 B7 B8 B15 B16 B28 B30 B34 CO-nC 8H 17 CO-nC 15H 31 CO 2-nHex CO 2-nC 10H 21 H H B3 B7 B8 B15 Me H CF 3 SCF 3 Me Me Me Et Me OMe Cl OCHF 2 CF 3 H Cl Me Me CN CF 3 CF 3 CF 3 CF 3 CF 3 Cl H Me Me Me Me Me Me nPr OMe Cl Me CF 3 H Cl Me Me Me Me Me Me Me Me
Table 12 (continuing)
G B Y 1 Y 2
4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBu 4-tBuCH 2 4-tBuCH 2 4-tBuCH 2 4-tBuCH 2 4-tBuCH 2 4-tBuCH 2 4-Et(Me) 2C B16 B28 B30 B16 B16 B17 B17 CO 2-nC 10H 21 CH 2OEt B7 B7 B7 B16 B3 2-(4-tBu-Ph)-3，3-Me 2-cPrC(O) B45 B3 B7 B16 B7 B8 B7 H CF 3 CF 3 CF 3 Cl CF 3 CF 3 Me CF 3 CF 3 Me Cl CN CN CN CF 3 CF 3 CF 3 Me Me CF 3 CF 3 Cl CF 3 Me Me Me Cl Me Me Me Me Me CF 3 Cl Me Me Me Me Me Me Me Me Me Me Me Me
Table 12 (continuing)
G B Y 1 Y 2
4-Et(Me) 2C 4-Et(Me) 2C 4-Et(Me) 2C 4-Et(Me) 2C 4-Et(Me) 2C 4-Et(Me) 2C 4-Et(Me) 2C 4-Et(Me) 2C 4-Et(Me) 2C 4-Et(Me) 2C 4-Et(Me) 2C 4-Et(Me) 2C 4-Et(Me) 2C 4-Et(Me) 2C 4-Et(Me) 2C 4-Et(Me) 2C 4-Et(Me) 2C 4-Et(Me) 2C 4-Et(Me) 2C 4-nHex 4-nHep 4-nOct 4-nNon B3 B7 B8 B34 B42 B16 B17 H B7 B8 B7 B7 B4 B5 B6 B3 B16 B17 B24 B34 B42 B43 B43 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Cl Cl Cl Me CN H Me Me Me Me Me Me CF 3 CF 3 Me Me Me Me Me Me Me Me Me Me Me Me CF 3 Me Me Me Me Cl Cl Cl Cl Me Me Me Me
Table 12 (continuing)
G B Y 1 Y 2
4-nDec 4-(Me) 2(CN)C 4-PhCH 2 4-Ph(Me) 2C 4-(4-F-Ph)(Me) 2C 4-MeCH＝CH 4-MeCC 3-CF 3 4-CF 3 4-CF 3 4-CF 3 4-CF 3 4-CF 3 4-CF 3 4-CF 3 4-CF 3 4-CF 3 4-CF 3 4-CF 3 4-CF 3CH 2 4-Cl 2C＝CHCH 2 4-BrCC 4-(2，2-F 2)cBuCH 2 H B7 B7 B7 B7 B4 B5 B6 B7 B8 B9 B16 B17 B16 B17 B7 B7 B7 B3 B7 B8 B7 B7 Cl Cl CF 3 CF 3 CN H Cl H OMe SMe SCF 3 Me Me Me Cl Cl CF 3 Me Cl Me Cl Cl CF 3 Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 12 (continuing)
G B Y 1 Y 2
4-(1-Me)cPr 4-cHex 4-(1-Me)cHex 4-MeO 4-iPrO 4-iPrO 4-iPrO 4-iPrO 4-iPrO 4-iPrO 4-iPrO 4-tBuO 4-tBuO 4-tBuO 4-nHexO 4-nOctO 4-nDecO 4-CH 2＝CHCH 2O 4-CHCCH 2O 4-CHF 2O 4-CHF 2O 4-CHF 2O 4-CHF 2O B16 B7 B8 B7 B7 B7 B15 B7 B16 B17 B23 B7 B8 B7 B8 B34 H B7 B8 B34 B7 B35 B36 CN CF 3 CF 3 CF 3 Cl CF 3 CF 3 Me Me Me SCF 3 Me CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Et Me Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 12 (continuing)
G B Y 1 Y 2
4-CHF 2O 4-CBrF 2O 4-CBrF 2O 4-CBrF 2O 4-CBrF 2O 4-CBrF 2O 4-CBrF 2O 4-CBrF 2O 4-CBrF 2O 4-CBrF 2O 4-CBrF 2O 4-CF 3O 4-CF 3O 4-CF 3O 4-CF 3O 4-CF 3O 4-CF 3O 4-CF 3CH 2O 4-CF 2＝CHCH 2CH 2O 4-CCl 2＝CHCH 2O 4-ClCCCH 2O 4-MeS 4-sBuS B7 B8 B34 B40 B41 B42 B7 B8 COCO 2Me H B1 B2 B3 B4 B5 B6 B7 B8 B9 B10 B11 B12 H CF 3 Cl Cl Me Me Cl CF 3 CF 3 CF 3 H CF 3 Cl H OMe SMe SCF 3 CF 3 Me Me Cl Cl CF 3 CF 3 Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 12 (continuing)
G B Y 1 Y 2
4-EtSO 4-MeSO 2 4-MeSO 2 4-MeSO 2 4-MeSO 2 4-EtSO 2 4-EtSO 2 4-iPrSO 2 4-iPrSO 2 4-tBuSO 2 4-tBuSO 2 4-MeCH＝CHCH 2S 4-CH 2＝CHCH 2SO 4-CH 2＝CHCH 2SO 2 4-CHCCH 2S 4-CHCCH 2SO 4-CHCCH 2SO 2 4-CHF 2S 4-CHF 2S 4-CHF 2S 4-CHF 2S 4-CHF 2S 4-CHF 2S B3 H B3 B32 B33 H B3 B32 B33 B7 B33 B15 B16 B28 B30 B34 CO-nC 8H 17 H B7 B8 B15 B29 H H CF 3 CF 3 CF 3 CF 3 CF 3 Et CF 3 CF 3 CF 3 CF 3 H OMe SMe SCF 3 Me Me CF 3 CF 3 CF 3 CF 3 CF 3 Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 12 (continuing)
G B Y 1 Y 2
4-CHF 2S 4-CHF 2S 4-CBrF 2S 4-CBrF 2S 4-CBrF 2S 4-CBrF 2S 4-CBrF 2S 4-CBrF 2S 4-CBrF 2S 4-CBrF 2S 4-CBrF 2S 4-CBrF 2S 4-CBrF 2S 4-CBrF 2S 4-CBrF 2S 4-CF 3S 4-CF 3S 4-CF 3S 4-CF 3S 4-CF 3S 4-CF 3S 4-CF 3S 4-CF 3S B7 B15 B7 B15 B30 B43 CO-nC 15H 31 CO 2-nHex H B7 B8 B15 B28 B34 B7 CO 2-nC 10H 21 H B3 B7 B8 B15 H B7 Me Me Me Me Me Me nPr CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Me Cl Me Me Me Me Me CF 3 CF 3 Me Me CF 3 CF 3 CF 3 CF 3 Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 12 (continuing)
G B Y 1 Y 2
4-CF 3S 4-CF 3S 4-CF 3S 4-CF 3S 4-CF 3S 4-CF 3S 4-CF 3S 4-CF 3CH 2S 4-CHF 2CF 2S 4-CHF 2SO 4-CBrF 2SO 4-CBrF 2SO 4-CBrF 2SO 4-CBrF 2SO 4-CBrF 2SO 4-CBrF 2SO 4-CF 3SO 4-CF 3SO 4-CF 3SO 4-CF 3SO 4-CF 3CH 2SO 2 4-CHF 2CF 2SO 2 4-CHF 2SO 2 B8 B15 B34 CO 2-nC 12H 25 CO-nC 15H 31 CO-nC 16H 33 CO-nC 17H 35 CO-nC 18H 37 CO-nC 19H 39 CO-nC 20H 41 H B3 B7 B24 B32 B33 H B3 B7 B33 B15 B16 B28 CF 3 CF 3 CF 3 CF 3 CF 3 Me Me CF 3 CF 3 Cl H CF 3 CF 3 CF 3 CF 3 CF 3 Me Me Me Me H OMe SMe Me Me Me Me Me Me Me Me Me Cl Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 12 (continuing)
G B Y 1 Y 2
4-CHF 2SO 2 4-CHF 2SO 2 4-CHF 2SO 2 4-CHF 2SO 2 4-CHF 2SO 2 4-CHF 2SO 2 4-CHF 2SO 2 4-CHF 2SO 2 4-CBrF 2SO 2 4-CBrF 2SO 2 4-CBrF 2SO 2 4-CBrF 2SO 2 4-CBrF 2SO 2 4-CBrF 2SO 2 4-CBrF 2SO 2 4-CBrF 2SO 2 4-CBrF 2SO 2 4-CBrF 2SO 2 4-CBrF 2SO 2 4-CBrF 2SO 2 4-CBrF 2SO 2 4-CBrF 2SO 2 4-CBrF 2SO 2 B7 B24 B32 B33 H B3 B7 B33 H B2 B3 B18 B19 B33 H B3 B7 B20 B32 B33 B37 B7 B15 CF 3 CF 3 CF 3 CF 3 Me Me Me Me SCF 3 Me Me Me Me Me CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me CF 3 CF 3
Table 12 (continuing)
G B Y 1 Y 2
4-CBrF 2SO 2 4-CBrF 2SO 2 4-CBrF 2SO 2 4-CF 3SO 2 4-CF 3SO 2 4-CF 3SO 2 4-CF 3SO 2 4-CF 3SO 2 4-CF 3SO 2 4-CF 3SO 2 4-CF 3SO 2 4-Cl 2C＝CHCH 2S 4-Cl 2C＝CHCH 2SO 4-Cl 2C＝CHCH 2SO 2 4-CBrCCH 2S 4-CBrCCH 2SO 4-CBrCCH 2SO 2 4-CHO 4-NO 2 4-CN 4-(Me) 2N 4-Me(MeCO)N 4-PhMeN B17 B7 B16 B16 B7 B15 B3 B7 B15 B7 B8 B16 B17 B17 CO 2-nC 10H 21 B33 B7 B7 B8 B16 B3 B7 B8 Me Me Me Me Cl Cl CF 3 CF 3 Me Me Me Me Me Cl Cl CF 3 CF 3 H H Cl H OMe SMe CF 3 CF 3 CF 3 Me Me Cl Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 12 (continuing)
G B Y 1 Y 2
4-PhCH 2(MeCO) N 4-(1-naphthyl) 4-(2-naphthyl) 4-(2-Cl-Ph) CH 2O 4-(3-Cl-Ph)CH 2O 4-(4-Cl-Ph)CH 2O 4-(4-Cl-Ph)CH 2O 4-(4-Cl-Ph)CH 2O 4-(4-F-Ph)CH 2O 4-(2-Me-Ph)CH 2O 4-(4-Me-Ph)CH 2O 4-(4-Et-Ph)CH 2O 3-(2，4-Cl 2-Ph)CH 2O 4-(3，4-Cl 2-Ph)CH 2O 4-(2，5-Me 2-Ph)CH 2O 4-(2，3，4，5，6-F 5-Ph)CH 2O 4-MeOC(O) 4-EtOC(O) 4-nPrOC(O) 4-iPrOC(O) 4-tBuOC(O) 4-tBuOC(O) 4-tBuOC(O) B15 B16 B28 B30 B34 B7 B7 B37 B42 B43 B43 H B7 B7 B7 B7 B4 B5 B6 B7 B7 B3 B5 SCF 3 Me Me Me Cl CF 3 Cl Cl CF 3 CF 3 CF 3 CF 3 CF 3 H OMe SMe SCF 3 Me Me Me Me CF 3 CF 3 Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 12 (continuing)
G B Y 1 Y 2
4-tBuOC(O) 4-tBuOC(O) 4-tBuOC(O) 4-tBuOC(O) 4-tBuOC(O) 4-tBuCH 2OC(O) 4-Et(Me) 2COC(O) 4-nHexOC(O) 4-MeOCH 2 4-EtOCH 2 4-iPrOCH 2 4-MeC(O) 4-EtC(O) 4-iPrC(O) 4-tBuC(O) 4-tBuC(O) 4-tBuC(O) 4-tBuC(O) 4-tBuC(O) 4-tBuC(O) 4-tBuC(O) 4-tBuC(O) 4-tBuC(O) B33 H B7 B8 B34 B10 B11 B7 B8 B7 B7 B16 B7 B8 H B3 B7 B3 B7 B15 B7 B17 B16 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 H H Cl H OMe SMe SCF 3 Cl Cl Cl CF 3 CF 3 CF 3 Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Cl Cl Cl Me Me Me Me Me Me
Table 12 (continuing)
G B Y 1 Y 2
4-CF 3C(O) 4-CF 3CF 2C(O) 4-CF 2CF 2CF 2C(O) 4-MeC(O)O 4-iPrC(O)O 4-tBuC(O)O 4-CF 3C(O)O 4-CF 2CF 2CF 2C(O)O 4-Me 2NC(O)O 4-Et 2NC(O)O 4-(nPr) 2NC(O)O 3-Ph 4-Ph 4-(4-F-Ph) 4-(4-F-Ph) 3-PhO 3-PhO 4-PhO 4-(4-F-Ph)O 4-(4-Cl-Ph)O 4-(4-Br-Ph)O 4-(4-Me-Ph) 4-(2-Cl-Ph)O B33 B8 B22 B23 B7 B8 B7 B8 B34 H B7 B8 B34 B7 B7 B7 B15 B7 B35 B36 B7 B8 B34 Me Me Cl Cl CF 3 CF 3 H H Cl H OMe SMe SCF 3 Et CF 3 Me CF 3 Me Me Et CF 3 CF 3 CF 3 Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 12 (continuing)
G B Y 1 Y 2
4-(2-F-Ph)O 4-(3-Cl-Ph)O 4-(4-Cl-Ph)O 4-(2，4-Cl 2-Ph)O 4-(3，4-Cl 2-Ph)O 4-(3，4，5-Cl 3-Ph) O 4-(2-Me-Ph) O 4-(4-Me-Ph) O 4-(3-Cl-4-Me-Ph) O 4-(2-pyridyl) 4-(5-CF 3-pyridine radicals-2-yl) 4-(2-pyridine radicals) O 4-(2-pyridine radicals) O 4-(2-pyridine radicals) O 4-(2-pyridine radicals) O 4-(2-pyridine radicals) O 4-(2-pyridine radicals) O 4-(5-CF3-pyridyl-2-yl) O 4-(5-CF 3-pyridyl-2-yl) O 4-(5-CF 3-pyridyl-2-yl) O 4-(5-CF 3-pyridyl-2-yl) O 4-(5-CF 3-pyridyl-2-yl) O 4-(5-CF 3-pyridyl-2-yl) O B40 B41 B42 B43 B44 COCO 2Me H B1 B2 B3 B4 B7 B15 B7 B8 B34 B5 B7 B8 B15 B7 B15 B34 H H Cl H OMe SMe SCF 3 Me H H Cl Me Me CF 3 CF 3 CF 3 CF 3 Me Me CF 3 CF 3 CF 3 CF 3 Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 12 (continuing)
G B Y 1 Y 2
4-(3-Cl-5-CF 3-pyridyl-2-yl) 4-(3-Cl-5-CF 3-pyridyl-2-yl) 4-(3-Cl-5-CF 3-pyridyl-2-yl) 4-(3-Cl-5-CF 3-pyridyl-2-yl) 4-(3-Cl-5-CF 3-pyridyl-2-yl) 4-(3-Cl-5-CF 3-pyridyl-2-yl) 4-(3-Cl-5-CF 3-pyridyl-2-yl) 4-(5-Cl-thiophene-2-yl) 3-OCH 2O-4 4-OCF 2O-4 4-MeCH＝N 4-Me 2C＝N 4-MeEtC＝N 4-PhCH＝N 4-PhMeC＝N 4-PhCH 2CH＝N 4-cC 6H 10＝N 3-CH 2CH 2CH 2-4 3-CH 2CH 2CH 2CH 2-4 4-PhC(O) 4-PhC(O) 4-PhC(O) 4-PhC(O) B7 B15 B34 B7 B15 B17 H B8 B9 B10 B11 B12 H B3 B7 B8 B15 B16 B28 H B7 B7 B33 Me Me Me CF 3 CF 3 CF 3 CF 3 Cl Cl CF 3 CF 3 CF 3 Cl Cl Cl CF 3 CF 3 CF 3 Cl CF 3 Et CF 3 CF 3 Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 12 (continuing)
G B Y 1 Y 2
4-(2-Cl-Ph)C(O) 4-(4-F-Ph)C(O) 4-(4-Cl-Ph)C(O) 4-(4-Cl-Ph)C(O) 4-(4-Cl-Ph)C(O) 4-(4-Me-Ph)C(O) 4-(4-Me-Ph)C(O) 4-(3，4-Cl 2-Ph)C(O) 2，4-Cl 2 3，4-Cl 2 4-Cl-2-F 3-Cl-4-nHex 4-tBu-3-Cl 4-tBu-3-Cl 3-Cl-4-iPrO 3-Cl-4-iPrO 3-Cl-4-nHepO 3-Cl-4-(3，4-Cl 2-PhCH 2)O 3-Cl-4-PhCH 2O 3-Cl-4-Me 3CCH 2 3，4-(MeO) 2 4-MeO-3-Me 4-OH-3，5-(tBu) 2 B7 H B7 B15 B34 B3 B16 B45 B7 B7 B7 B7 B7 B15 B7 B7 B15 H B7 B7 B7 B17 B3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Me CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me Me
Table 12 (continuing)
G B Y 1 Y 2
3，4，5-Cl 3 3，5-Cl 2-4-F 4-Cl-2，6-F 2 2，6-F 2-4-CF 3 2，6-F 2-4-CF 3O 3，5-Cl 2-4-nOct 3，5-Cl 2-4-PhCH 2O 2，3，5，6-F 4-4-Me 2，3，4，5，6-F 5 B15 B7 B7 B7 B7 B7 B15 B3 B33 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 CF 3 Me Me Me Me Me Me Me Me Me
Table 13
Table 13 (continuing)
R 1 B A
2-F-Ph 2-F-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Me-Ph 2-Me-Ph 2-Me-Ph 4-NO 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph 2-pyridyl 2-pyridyl 2-pyridyl 2-pyridyl 2-pyridyl B5 B6 B7 B8 B15 B16 B17 B22 B31 B32 B33 B34 B35 B36 B40 B41 pyridine-2-base-C (O) pyridine-2-base-C (O) pyridine-2-base-C (O) B8 B15 B16 B17 4-Me-1,2,3-triazol-1-yl 5-Me-1,2,3-triazole-2-base 4-MeO 2C-1,2, the 3-triazole-, 1-1-base 4,5-EtO 2C-1,2,3-triazole-2-base 4,5-Me 2-1,2,3-triazoles-1-1-base 4,5-(MeO 2C) 2-1,2,3-triazoles-2-base 4,5-Me 2-1,2,4-triazole-4-base 2,4-Me 2-1,2,4-triazole-4-base 1,5-Me 2-1,2,4-triazole-3-base 5-Me-3-CF 3-1,2,4-triazole-2-base 3-Cl-5-CF 3-1,2,4-triazole-2-base 5-Cl-3-CF 3-1,2-4-triazole-2-base 3,5-Me 31,2-4-triazole-4-base 3,5-Cl 2-1,2-4-triazole-4-base 3,5-(CF 3) 2-1,2-4-triazole-4-base 5-tetrazyl 5-Ph-1-tetrazyl 5-Ph-2-tetrazyl 3,4,4,5-Me 4-2-pyrazoline-1-base 3-Me-5-CF 3-2-pyrazoline-1-base 1,5-Me 2-3-CF 3-2-pyrazoline-4-base 1,4-Me 2-3-Ph-2-pyrazoline-4-base 1,4-Me 2-5-Ph-2-pyrazoline-4-base
R 1 B A
iPr iPr tBu tBu tBu 1-Me-cPr 1-Me-cPr 1-Me-cPr 1-Me-cPr 1-Me-cHex 1-Me-cHex 1-Me-cHex 1-Me-cHex PhCH 2 PhCH 2 PhCH 2 PhMe 2C PhMe 2C PhMe 2C PhMe 2C Ph 2-F-Ph 2-F-Ph H B3 B5 B6 B7 B8 B15 B16 B17 B22 B31 B32 B33 B34 B35 B36 B40 B41 pyridine-2-base-C (O) pyridine-2-base-C (O) pyridine-2-base-C (O) H B3 2，5-Me 2-1-pyrryl 1-Me-2-pyrrolyl 3,5-Me 2-2-pyrryl 3,4-Me 2-2-pyrryl 3,4,5-Me 3-2-pyrryl 3,5-Me 2-4-MeO-2-pyrryl 4-MeC (O)-3,5-Me 2-2-pyrryl 4-NO 2-2-pyrryl 2-Me-3-pyrryl 4-Me-3-pyrryl 2,4,5-Me 33-pyrryl 2,4-Me 2-5-EtO 2C-3-pyrryl 1,2,3-triazole-4-base 1-Me-1,2,3-triazole-4-base 2-Me-1,2,3-triazole-4-base 3-Me-1,2,3-triazole-4-base 2-EtO 2C-1,2,3-triazole-4-base 5-Me-2-Ph-1,2,3-triazole-4-base 5-CF 3-2-Me-1,2,3-triazole-4-base 2,5-Me 2-1,2,3-triazoles-4-base 1-PhCH 2-5-Me-1,2,3-triazole-4-base 1-PhCH 2-5-CF 3-1,2,3-triazoles-4-base 1-PhCH 2-5-Cl-1,2,3-triazole-4-base
Table 13 (continuing)
R 1 B A
2-pyridine radicals 1-naphthyl 1-naphthyl 1-naphthyl iPr iPr tBu 1-Me-cPr cHex 1-Me-cHex PhCH2 PhMe 2C Ph 2-F-Ph 2-Cl-Ph 2-Me-Ph 4-NO 2-Ph 2，6-F 2-Ph 2，6-Cl 2-Ph 2-pyridyl 1-naphthyl B22 B31 B32 B33 B34 B35 B36 B40 B41 pyridine radicals-2-base-C (O) pyridine radicals-2-base-C (O) pyridine radicals-2-base-C (O) B8 B15 B16 B17 B22 B31 B32 B33 B34 1，3-Me 2-2-pyrazoline-5-base 1,5-Me 2-2-pyrazoline-3-base 2-Me-2-tetrahydroglyoxaline-1-base 2-CF 3-2-tetrahydroglyoxaline-1-base 2-MeS-2-tetrahydroglyoxaline-1-base 2-MeO-2-tetrahydroglyoxaline-1-base 5-Me-2-Ph-2-oxazoline-4-base 2,5-Me 2-2-oxazoline-4-base 5-Me-2-CF 3-2-oxazoline-4-base 2-thiazoline-2-base 2-Me 2N-2-thiazoline-4-base 2,4-Me 2-2-thiazoline-4-base 2-Me-4-CF 3-2-thiazoline-5-base 5-Me-2-isoxazoline-3-base 3-Cl-5-Me-2-isoxazoline-3-base 3,5-(MeS) 2-2-isoxazoline-4-base 5-Cl-2-Me-3 (2H)-pyridazinone-4-base yl 5,6-Cl 2-2-Me-pyridazinone-4-base yl 4-Cl-2-Me-pyridazinone-4-base yl 4,6-Cl 2-2-Me-pyridazinone-4-base yl 4,5-Cl 2-2-Me-pyridazinone-4-base yl
Table 14
Figure C9719404103042
Or
R 1 E B A
tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu tBu 2，6-F 2-Ph tBu tBu tBu tBu 2，6-F 2-Ph 2，6-F 2-Ph Oxazole-2-base thiazol-2-yl imidazoles-2-base 1,5-Me 2-1,2,4-triazole-3-base 5-Me-1,2,4-oxadiazole-3-base 5-CF 3-1,2,4-thiadiazoles-3-base 5-Me-1,3,4-oxadiazole-2-base tetrazolium-5-base 2-oxazoline-2-base 1,2,4,5-tetrazine-3-base F Cl Br I CHC CHC CHC MeCC EtCC PhCC PhCC PhCC PhCC H B3 B7 B8 B15 B16 B17 B18 B32 B33 B34 H B7 B8 H B7 B7 B7 B7 B7 B8 H B7 A1 A2 A3 A4 A5 A6 A7 A8 A9 A10 A11 A12 A13 A14 A15 A2 A2 A16 A17 A2 A13 A2 A2
Table 14 (continuing)
R 1 E B A
Pyridine-2-base tBu tBu 2,6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph tBu tBu pyridyl-2-base 2,6-F 2-Ph 2，6-F 2-Ph PhCC (2-Cl-Ph)CC (3-Cl-Ph)CC (4-Cl-Ph)CC (4-F-Ph)CC (4-Me-Ph)CC (4-nHex-Ph)CC (2，6-Cl 2-Ph)CC (2，4-Cl 2-Ph)CC (3，4-Cl 2-Ph)CC (2，4，6-Me 3-Ph)CC (4-CF 3-Ph)CC CF 3 CF 3CF 2 NO 2 N 3 N 3 N 3 N 3 N 3 N 3 CHO C(O)Me B7 B15 B15 B16 B17 B18 B34 H (EtO) 2P(S) B3 B7 B15 B7 H B3 B7 H B7 B7 H B7 B8 B15 A2 A19 A20 A21 A22 A23 A24 A25 A26 A27 A28 A29 A2 A31 A32 A33 A2 A1 A2 A2 A2 A34 A35
Table 14 (continuing)
R 1 E B A
2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph tBu tBu tBu tBu tBu 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph pyridine radicals-2-yl pyridines base-2-yl pyridines base-2-base tBu tBu tBu tBu 2,6-F2-Ph C(O)Et C(O)iPr C(O)nBu C(O)sBu C(O)tBu C(O)tBu C(O)tBu C(O)tBu C(O)tBu CO 2Me CO 2Me CO 2Me CO 2Me CO 2Me CO 2Me CO 2Me CO 2Me CO 2Me CO 2Me CO 2Et CO 2Et CO 2Et CO 2Et B16 B17 B18 B32 H H B7 H B7 H B7 B8 H B7 B8 H B7 B8 B34 H B7 B8 H A36 A1 A2 A3 A2 A1 A1 A2 A2 A2 A2 A2 A2 A2 A2 A2 A2 A2 A5 A2 A2 A2 A2
Table 14 (continuing)
R 1 E B A
2，6-F 2-Ph 2，6-F 2-Ph pyridine radicals-2-yl pyridines base-2-yl pyridines base-2-yl pyridines base-2-yl pyridines base-2-yl pyridines base-2-yl pyridines base-2-yl pyridines base-2-yl pyridines base-2-yl pyridines base-2-yl pyridines base-2-yl pyridines base-2-base tBu tBu tBu 2,6-F2-Ph 2，6-F 2-Ph 2，6-F 2-Ph pyridyl-2-base 2,6-F 2-Ph tBu CO 2Et CO 2Et CO 2Et CO 2Et CO 2Et CO 2Et CO 2nPr CO 2iPr CO 2nBu CO 2iBu CO 2sBu CO 2tBu CO 2CH 2CH＝CH 2 CO 2CH 2CH＝CH 2 CO 2CH 2CH＝CH 2 CO 2CH 2CH＝CH 2 CO 2CH 2CH＝CH 2 CO 2CH 2CH＝CH 2 CO 2CH 2CH＝CH 2 CO 2CH 2CH＝CH 2 C(O)NHMe C(O)NHMe C(O)NHMe B7 B8 H B7 B8 H B7 B8 H B7 B7 B8 B15 B7 B8 H B7 B8 H B7 B8 H H A2 A2 A2 A2 A2 A6 A7 A8 A9 A10 A11 A12 A13 A2 A2 A2 A2 A2 A2 A2 A2 A2 A2
Table 14 (continuing)
R 1 E B A
Pyridine radicals-2-yl pyridines base-2-base tBu tBu tBu tBu tBu tBu 2,6-F2-Ph pyridyl-4-base 2,6-F 2-Ph tBu tBu tBu tBu tBu 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph pyridyl-2-yl pyridines base-2-base 2,6-F 2-Ph 2，6-F 2-Ph C(O)NHEt C(O)NHnPr C(O)NHiPr C(O)NHiBu C(O)NHtBu C(O)NMe 2 C(O)NMe 2 C(O)NMe 2 C(O)NMe 2 C(O)NMeEt C(O)NEt 2 C(O)N(nPr) 2 PhC(O) PhC(O) PhC(O) PhC(O) PhC(O) PhC(O) PhC(O) PhC(O) PhC(O) (4-F-Ph)C(O) (3，4-Cl 2-Ph)C(O) B16 B17 B18 B34 H (EtO) 2P(S) H B7 B7 B3 B7 B15 H H B7 B8 H B7 B8 H B7 B8 H A15 A16 A17 A18 A19 A20 A2 A2 A2 A21 A22 A23 A24 A2 A2 A2 A2 A2 A2 A2 A2 A2 A6
Table 14 (continuing)
R 1 E B A
Pyridin-3-yl pyridin-3-yl tBu tBu tBu 2,6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph pyridyl-2-yl pyridines base-2-base 2,6-F 2-Ph 2，6-F 2-Ph pyridyl-2-yl pyridines base-2-base tBu tBu tBu 2,6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph pyridyl-2-yl pyridines base-2-base tBu (3-Cl-4-F-Ph)C(O) (4-Me-Ph)C(O) C(S)NH 2 C(S)NH 2 C(S)NH 2 C(S)NH 2 C(S)NH 2 C(S)NH 2 C(S)NH 2 C(S)NH 2 MeS EtS nPrS tBuS MeSO EtSO nPrSO tBuSO MeSO 2 EtSO 2 iPrSO 2 nBuSO 2 PhS B8 B15 B16 H B7 B8 H B7 B8 H B7 B18 B32 B33 B34 H B7 B8 H B7 B7 B8 B15 A27 A28 A29 A2 A2 A2 A2 A2 A2 A2 A2 A31 A32 A33 A34 A35 A36 A1 A2 A3 A4 A5 A6
Table 14 (continuing)
R 1 E B A
tBu tBu 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph pyridine-2-yl pyridines-2-yl pyridines-2-base tBu tBu tBu 2,6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph pyridine-2-yl pyridines-2-base tBu tBu tBu PhS PhS PhS PhS PhS PhS PhS PhS (4-Me-Ph)S (4-Cl-Ph)SO (2-F-Ph)SO 2 (MeO) 2P(O) (EtO) 2P(O) (nPrO) 2P(O) (PhO)(MeO)P(O) (MeO) 2P(S) (EtO) 2P(S) (nPrO) 2P(S) (PhO)(MeO)P(S) H B7 B8 H B7 B8 H B7 B8 H B17 B18 B34 H (EtO) 2P(S) B3 B7 B15 B7 A2 A2 A2 A2 A2 A2 A2 A2 A2 A6 A9 A10 A11 A12 A13 A14 A15 A16 A17
With regard to The compounds of this invention was used as the situation of pesticides, usually, they can mix with suitable carriers, and described carrier is solid carrier for example, as clay, talcum, wilkinite, diatomite or white carbon; Or liquid vehicle, as water, alcohol (as Virahol, butanols, benzylalcohol, furfuryl alcohol), aromatic hydrocarbons (as toluene, dimethylbenzene), ether (as phenylmethylether), ketone (as pimelinketone, isophorone), ester (as butylacetate), acid amides (as N-Methyl pyrrolidone) or halohydrocarbon (as chlorobenzene); Randomly also can with other additive, be mixed together as tensio-active agent, emulsifying agent, dispersion agent, permeate agent, spreading agent, thickening material, freezing inhibitor, anti-hard caking agent and stablizer, and can be mixed with any actual application target thing form, as liquid preparation, emulsion, water absorbability pulvis, dried flowing agent, flowing agent, pulvis and granula.
With regard to The compounds of this invention is used the situation of used as pesticides, when it being mixed with the preparation that is used for actual use or actual in spraying or similar approach when using, they can combine with any other weedicide, various insecticide, nematocides, mycocide, crop growth regulator, synergistic agent, fertilizer and soil improvement agent.
Particularly, The compounds of this invention and other agricultural chemicals or the favourable part of plant hormone bonded are: the amount of used pharmaceutical chemicals can reduce, cause the reduction of processing cost thus, and the blended pharmaceutical chemicals has also represented the collaborative effectiveness of widening insecticidal spectrum when demonstrating higher insecticidal activity.In case of necessity, The compounds of this invention can combine with many known agricultural chemicals.Can with The compounds of this invention bonded agricultural chemicals for example, at agrochemicals handbook (Farm ChemicalsHandbook), the compound described in 1994.
The dosage of The compounds of this invention depends on application position, time of application, application process, raise crop etc.Usually, with regard to activeconstituents, described dosage per hectare is approximately between 0.005kg and the 50kg.
Now, hereinafter will enumerate the formulation examples that contains The compounds of this invention, still, scope of the present invention is not to be limited to this.In following example of formulations, " part " is by weight.
[water absorbability pulvis]
5 to 80 parts of The compounds of this invention
10 to 85 parts of solid carriers
1 to 10 part in tensio-active agent
Other 1 to 5 part
Other comprises: anti-hard caking agent etc. for example.
[emulsion]
1 to 30 part of The compounds of this invention
30 to 95 parts of liquid vehicles
5 to 15 parts in tensio-active agent
[flowing agent]
5 to 70 parts of The compounds of this invention
15 to 65 parts of liquid vehicles
5 to 12 parts in tensio-active agent
Other 5 to 30 parts
Other comprises: for example antithrombotics, thickening material etc.
[dried flowing agent (water absorbability particle)]
20 to 90 parts of The compounds of this invention
10 to 60 parts of solid carriers
1 to 20 part in tensio-active agent
[granula]
0.1 to 10 part of The compounds of this invention
90 to 99.99 parts of solid carriers
Other 1 to 5 part
[pulvis]
0.01 to 30 part of The compounds of this invention
67 to 99.5 parts of solid carriers
Other 0 to 3 part
Adhere to the near speech of the situation that prevents agent with regard to The compounds of this invention as hydrobiont, they can be mixed with various formulations, as applying agent, solution, emulsion, ball or thin slice to be applied to various objects.According to application position, object and form, described preparation can be any usual manner use, for example apply, spray, flood, add in the entry or be placed in the water.Above-mentioned coating agent, solution, emulsion or other preparation can use any ordinary method to finish.Except the formulation and mode of above-mentioned use The compounds of this invention, can also use The compounds of this invention in the following manner, for example, when manufacturing is used for the rope of fishing net and filamentary material, this compound is added in rope and the filamentary material, make it have the ability that prevents that hydrobiont from adhering to.Hydrobiont of the present invention adheres to and prevents that agent from both can use separately, also can adhere to any other hydrobiont to prevent that agent is used in combination.
When using hydrobiont of the present invention to adhere to the form of antifouling coating to prevent agent, for example, The compounds of this invention and membrane-forming agent can be mixed and made into coating.Described membrane-forming agent comprises paint, synthetic resins, synthetic chloroprene rubber etc.In case of necessity, also can add solvent, pigment and other material.With regard to making coating, the highest limit of The compounds of this invention concentration is had no particular limits, can this condition of film forming as long as satisfy the coating that generates, but, for the weight of antifouling coating, the concentration of The compounds of this invention can be 1 to 50 weight %, preferred 5 to 20 weight %.
When using hydrobiont of the present invention to adhere to the form of solution to prevent agent, for example, The compounds of this invention can be dissolved in solvent with membrane-forming agent and make solution.Described membrane-forming agent comprises synthetic resins, synthetic chloroprene rubber, natural rubber etc.Described solvent comprises dimethylbenzene, toluene, cumene, butanone, methyl iso-butyl ketone (MIBK), acetone etc.In case of necessity, also additive can be added solution as softening agent.With regard to making solution, the highest limit of The compounds of this invention concentration is had no particular limits, can dissolve this compound and make this condition of solution as long as satisfy, but, for the weight of solution, the concentration of The compounds of this invention can be 1 to 50 weight %, preferred 5 to 30 weight %.
When using hydrobiont of the present invention to adhere to emulsion form to prevent agent, tensio-active agent is added The compounds of this invention make the emulsion of being planned according to the ordinary method of the general emulsion of preparation.Wherein, the type to used tensio-active agent is not particularly limited.With regard to making emulsion, the highest limit of The compounds of this invention concentration is had no particular limits, can make this condition of emulsion by this compound of emulsification as long as satisfy, but, for the weight of emulsion, the concentration of The compounds of this invention can be 1 to 50 weight %, preferred 5 to 30 weight %.
When using hydrobiont of the present invention to adhere to ball or sheet form to prevent agent, for example, at room temperature, The compounds of this invention component and optional softening agent, tensio-active agent and other material are added in the solid hydrophilic resinous substrates (as the polyoxyethylene glycol that exists with solid form), and the mixture that generates is made ball shape or thin slice by melt-forming, compression moulding or similar approach.With regard to making ball or thin slice, the highest limit to The compounds of this invention concentration has no particular limits, as long as satisfy and this compound can be shaped to ball shape or laminar this condition, but, weight for ball or thin slice, the concentration of The compounds of this invention can be 25 to 90 weight %, preferred 30 to 90 weight %.
[embodiment]
Below, specify the present invention by synthetic embodiment, example of formulations and experimental example, still, scope of the present invention is not limited in this.
[synthetic embodiment 1]
2-{3-(2, the 6-difluorophenyl) pyrazol-1-yl }-3-(1-methyl-3,5-dichloro pyrazoles-4-yl)-3-hydroxyl vinyl cyanide (Compound I-40) synthetic:
1) 3.0g 3-(2, the 6-difluorophenyl) pyrazoles is dissolved in the 20ml acetonitrile, at room temperature, 2.52g chloromethyl cyanide and 4.61g salt of wormwood is added wherein, and under the backflow situation, heated 5 hours.After removing acetonitrile under reduced pressure, ethyl acetate is added resistates, then, resistates is washed with a small amount of.Use the dried over sodium sulfate organic layer, and remove solvent under reduced pressure.From mixed solvent: recrystallization goes out residual product and obtains 1.74g 1-cyano methyl-3-(2, the 6-difluorophenyl) pyrazoles isopropyl ether and the ether.
2) under 50 ℃, 0.5g 1-cyano methyl-3-(2, the 6-difluorophenyl) pyrazoles is dissolved in the formed solution of 10mlTHF dropwise adds 0.15g 55% sodium hydride in 10ml THF in the formed suspension.To generate product and stir after 30 minutes, and under 50 ℃, again 0.67g 1-(1-methyl-3,5-dichloro pyrazoles-4-carbonyl) pyrazoles will be dissolved in the formed solution of 10ml THF and dropwise add wherein, then, at room temperature, stirring is spent the night.Reaction mixture is poured in the water, washed with ethyl acetate extraction with less water then.With the product of dried over sodium sulfate generation, and remove solvent under reduced pressure.From mixed solvent: recrystallization goes out residual product and obtains 0.52g2-{3-(2, the 6-difluorophenyl) pyrazol-1-yl isopropyl ether/ethyl acetate=3/1 }-3-(1-methyl-3,5-dichloro pyrazoles-4-yl)-3-hydroxyl vinyl cyanide.
[synthetic embodiment 2]
Synthesizing of 3-(1-methyl-3,5-dichloro pyrazoles-4-yl)-2-(2-phenyl thiazole-4-yl)-3-hydroxyl vinyl cyanide (Compound I I-1):
1) the 2.33g thiobenzamide is dissolved in the 20ml anhydrous methanol, and at room temperature, with 2.16g1, the 3-Dichloro acetone adds wherein, then, heating is 1 hour under the backflow situation.Remove solvent under reduced pressure, and frozen water is added resultant product, then, neutralize with sodium bicarbonate aqueous solution.With the product ethyl acetate extraction that generates, with the saturated brine washing, and use dried over sodium sulfate, remove solvent again under reduced pressure.Residual product by purification by silica gel column chromatography, is obtained 2.03g 4-chloromethyl-2-phenyl thiazole from the flow point with chloroform/normal hexane=1/2 wash-out.
2) 1.39g 4-chloromethyl-2-phenyl thiazole is dissolved in the 10ml acetonitrile, and at room temperature, 0.65g potassium cyanide and 0.05g dibenzo-18-hat-6-ether is added wherein, then, heating is 10 hours under situation about refluxing.After temperature is got back to room temperature, ethyl acetate is added in the mixture that generates, and by removing by filter insoluble solids.With ethyl acetate solution saturated brine and the water washing that produces, and use dried over sodium sulfate, remove solvent again under reduced pressure.Residual product by purification by silica gel column chromatography, is obtained 0.98g 4-cyano methyl-2-phenyl thiazole from the flow point with the chloroform wash-out.
3) 0.72g 4-cyano methyl-2-phenyl thiazole is dissolved in the anhydrous THF of 10ml, in argon gas atmosphere,, 4.6ml n-Butyl Lithium (1.56M hexane solution) is dropwise added wherein at-60 ℃ or more under the low temperature.At-60 ℃ or more under the low temperature, stir and generate product after 20 minutes, at-60 ℃ or more under the low temperature, with 0.84g 1-methyl-3,5-dichloro pyrazoles-4-formyl chloride is dissolved in the formed solution of the anhydrous THF of 3ml and dropwise adds wherein.Then, will generate product and heat gradually, and at room temperature stir 4 hours.Pour reaction mixture into frozen water, use the dilute hydrochloric acid acidifying, use ethyl acetate extraction, and wash with saturated brine.With the product that dried over sodium sulfate generated, and remove solvent under reduced pressure.Resultant product by purification by silica gel column chromatography, is obtained required product from the flow point with the chloroform wash-out.To generate product and obtain 0.86g 3-(1-methyl-3,5-dichloro pyrazoles-4-yl)-2-(2-phenyl thiazole-4-yl)-3-hydroxyl vinyl cyanide with ether crystallization and washing.
[synthetic embodiment 3]
3-(1-methyl-3-trifluoromethyl-5-chlorine pyrazoles-4-yl)-2-(4-tertiary butyl thiazole-2-yl)-3-new pentane acyloxy vinyl cyanide (compound III-6, III-15) synthetic:
At room temperature, 0.5g 3-(1-methyl-3-trifluoromethyl-5-chlorine pyrazoles-4-yl)-2-(4-tertiary butyl thiazole-2-yl)-3-hydroxyl vinyl cyanide and 0.14g triethylamine are added among the 15ml THF, and stirring obtains homogeneous solution.Under with ice-cooled situation, dropwise the 0.16g pivalyl chloride is added this solution, heating gradually then, and at room temperature stirred 8 hours.Pour reaction mixture into frozen water, use ethyl acetate extraction, and wash three times with saturated brine.After dried over sodium sulfate, make the short column of the product of generation by filling gel.Remove solvent under reduced pressure, and make residual product pass through silica gel thin-layer chromatography (developping agent: chloroform) obtain 0.16g 3-(1-methyl-3-trifluoromethyl-5-chlorine pyrazoles-4-yl)-2-(4-tertiary butyl thiazole-2-yl)-3-new pentane acyloxy vinyl cyanide (III-6) and its geometrical isomer of 0.35g (III-15).
Compound III-6:
1H-NMR(CDCl 3，δppm)；1.18(9H，s)，1.32(9H，s)，
3.85(3H，s)，6.88(1H，s)
Compound III-15:
1H-NMR(CDCl 3，δppm)；1.33(9H，s)，1.39(9H，s)，
3.94(3H，s)，7.03(1H，s)
[reference example]
Synthesizing of 1-methyl-3-trifluoromethyl-5-chlorine pyrazoles-4-carboxylic acid:
1) at 10 ℃ or more under the low temperature, dropwise the 21.35g phosphoryl chloride is added among the 4.72g DMF.After the temperature of reaction soln is got back to room temperature, stirred this reaction mixture 1 hour, and 10.71g1-methyl-3-trifluoromethyl-5-pyrazolone is added wherein.The mixture to 110 that heating generates ℃, and stirred 7 hours.After leaving standstill under 70 ℃, pour reaction mixture into frozen water.After making the pH of this mixture be approximately 4 with the aqueous sodium hydroxide solution that adds, the crystal that is settled out come out by filtering separation and dry, obtain 10.55g 1-methyl-3-trifluoromethyl-5-chlorine pyrazoles-4-formaldehyde.
2) at room temperature, 8.88g 1-methyl-3-trifluoromethyl-5-chlorine pyrazoles-4-formaldehyde and 7.24g potassium permanganate are added the aqueous solution that 0.23g potassium hydroxide forms in 85ml water.Be heated to temperature up to 60 ℃ after, the mixture that stir to generate 2 hours.Then, make the temperature of this mixture get back to room temperature, and pass through solids removed by filtration.The filtrate that generates with the aqueous hydrochloric acid acidifying, and the crystal that is settled out come out by filtering separation washes with water and dry again.The crystal that obtains is thus added in the 150ml chloroform, under the backflow situation, heats, and when hot by removing by filter insoluble solids.Remove chloroform under reduced pressure, obtain 6.24g 1-methyl-3-trifluoromethyl-5-chlorine pyrazoles-4-carboxylic acid.
[synthetic embodiment 4]
Synthesizing of 2-(2-tertiary butyl thiazole-4-yl)-3-(2-methyl-4-trifluoromethyl thiazole-5-yl)-3-benzoyloxy vinyl cyanide (Compound I I-75):
Described compound (viscous liquid, E-Z mixture) is synthetic with above-mentioned same method.
1H-NMR(CDCl 3，δppm)；1.09(9H，s)，2.75(3H，s)，
7.3-7.6(4H，m)，8.05-8.25(2H，m)：
Main component
1.19(9H，s)，2.70(3H，s)，
7.3-7.6(4H，m)，8.05-8.25(2H，m)：
Submember
[synthetic embodiment 5]
Synthesizing of 2-(4-trifluoromethyl)-3-(1-methyl-3,5-dichloro pyrazoles-4-yl)-3-(1-methyl-3,5-dichloro pyrazoles-4-carbonyl oxygen base) vinyl cyanide (compound IV-5):
With 1.0g 4-(trifluoromethyl) phenyl vinyl cyanide and 2.31g 1-methyl-3,5-dichloro pyrazoles-4-formyl chloride is dissolved in the anhydrous THF of 30ml, and at room temperature, adds the 0.61g potassium tert.-butoxide.After the heating, the product that generates is continued heating 3 hours under the backflow situation.Add the 0.61g potassium tert.-butoxide once more, and further under the backflow situation, heated 2 hours.Remove THF under reduced pressure, and water is added resultant product, then, use ethyl acetate extraction.After the organic layer that generates washed with the aqueous sodium hydroxide washes of alkene, wash with water again, then, it is used dried over sodium sulfate, and remove solvent under reduced pressure.Resultant product is passed through purification by silica gel column chromatography, from normal hexane: obtain 1.92g 3-(1-methyl-3 flow point of ethyl acetate=2: 1 wash-out, 5-dichloro pyrazoles-4-yl)-2-(4-trifluoromethyl)-3-(1-methyl-3,5-dichloro pyrazoles-4-carbonyl oxygen base) vinyl cyanide.
[synthetic embodiment 6]
Synthesizing of 2-(4-tert-butyl-phenyl)-3-(1-methyl-3,5-dichloro pyrazoles-4-yl)-3-hydroxyl vinyl cyanide (compound IV-18):
0.22g dibenzo-18-hat-6-ether and 1.57g sodium cyanide are suspended in 20ml DMSO, and under with water-cooled situation, dropwise 5.00g 4-tertiary butyl bromotoluene are added wherein.After at room temperature stirring is spent the night, under 50 ℃, the mixture that restir generates 5 hours.Then, at room temperature leave standstill, add entry, and use extracted with diethyl ether.Organic layer is washed with water, and use dried over sodium sulfate, remove solvent again under reduced pressure.With resultant product by purification by silica gel column chromatography, from normal hexane: obtain 1.19g 4-tert-butyl-phenyl vinyl cyanide the flow point of ethyl acetate=5: 1 wash-out.
With 1.00g 4-tert-butyl-phenyl vinyl cyanide and 1.23g 1-methyl-3,5-dichloro pyrazoles-4-formyl chloride is dissolved in 20ml THF, and under with ice-cooled situation, adds the 1.01g potassium tert.-butoxide.After at room temperature the mixture stirring that generates being spent the night, water is added wherein, then, use the dilute hydrochloric acid acidifying, and use ethyl acetate extraction.After organic layer washed with water, use dried over sodium sulfate, and remove solvent under reduced pressure.Residual product is dissolved in the mixed solvent that is formed by 10ml water and 10ml diox, adds 0.38g potassium hydroxide, and under situation about refluxing, heated 4 hours.After at room temperature leaving standstill, use the dilute hydrochloric acid acidifying again, and use ethyl acetate extraction.After organic layer washed with water, use dried over sodium sulfate, remove solvent again under reduced pressure.With residual product by purification by silica gel column chromatography, from normal hexane: obtain 0.64g 2-(4-tert-butyl-phenyl)-3-(1-methyl-3,5-dichloro pyrazoles-4-yl)-3-hydroxyl vinyl cyanide the flow point of ethyl acetate=2: 1 wash-out.
[synthetic embodiment 7]
Synthesizing of 2-(4-tert-butyl-phenyl)-3-(1-methyl-3-trifluoromethyl-5-chlorine pyrazoles-4-yl)-3-new pentane acyloxy vinyl cyanide (compound IV-24):
Described compound (viscous liquid) is synthetic with above-mentioned same method.
1H-NMR(CDCl 3，δppm)；1.13(9H，s)，1.33(9H，s)，
3.98(3H，s)，7.48(4H，brs)
[synthetic embodiment 8]
Synthesizing of 2-(4-tert-butyl-phenyl)-3-(3,5-two chloro-1-methyl-pyrazol-4-yls)-3-methoxyl group carbonyl oxygen base vinyl cyanide (compound IV-36):
Described compound (vitreousness, E-Z mixture) is synthetic with above-mentioned same method.
1H-NMR(CDCl 3，δppm)；1.32(9H，s)，3.75(3H，s)，
3.87(3H，s)，7.49(2H，d，J＝8Hz)，
7.58(2H，d，J＝8Hz)：75％
1.27(9H，s)，3.88(3H，s)，
3.96(3H，s)，7.49(2H，d，J＝8Hz)，
7.58(2H，d，J＝8Hz)：25％
[synthetic embodiment 9]
Uncle 2-{2-Ding Ji oxazole-4-yl }-3-(3,5-two chloro-1-methyl-pyrazoles-4-yls)-3-hydroxyl vinyl cyanide (compound V-40) synthetic:
1) with 25g pivalyl amine and 25g 1,3-two chloro-2-acetone mix, and under 135 ℃, heating is 2.5 hours in oil bath.After ice-cooled, make this compound become alkalescence by adding aqueous sodium hydroxide solution.Then.With the product that generates with ethyl acetate extraction after, wash with water, and use dried over sodium sulfate, remove solvent again under reduced pressure.Residual product is passed through column chromatography (silica gel; Ethyl acetate: normal hexane=1: 8) purifying obtains the 17.5g 2-tertiary butyl-4-Lv Jia Ji oxazole.
2) weigh up the 6.2g sodium cyanide, add the 50ml dimethyl sulfoxide (DMSO), dropwise add the dimethyl sulphoxide solution of the 16.9g 2-tertiary butyl-4-Lv Jia Ji oxazole again; And under 65 ℃, under condition of stirring, heating is 1 hour in the oil bath.After the product that generates is cooled to room temperature, adds the rare aqueous sodium hydroxide solution of 150ml, and extract with toluene.With organic layer water thorough washing, and use dried over sodium sulfate, remove solvent again under reduced pressure, obtain the 14.8g 2-tertiary butyl-4-Qing base Jia Ji oxazole.
3) the 2.87g potassium tert.-butoxide is suspended among the 20ml THF; Under with ice-cooled situation, dropwise with the 2.00g 2-tertiary butyl-4-cyanogen base first base oxazole and 2.37g 3,5-two chloro-1-methylpyrazole-4-formyl chlorides formed solution in 10ml THF adds wherein; Then, at room temperature, stirring is spent the night.Reaction mixture is poured in the frozen water, used ethyl acetate extraction, and wash with less water.With the product that generates with anhydrous sodium sulfate drying after, remove solvent under reduced pressure.Residual product is passed through column chromatography (silica gel; Normal hexane: ethyl acetate=4: 1) purifying obtains 3.26g purpose compound.
[synthetic embodiment 10]
Synthesizing of 2-(uncle 2-Ding Ji oxazole-4-yl)-3-(5-chloro-1-methyl-3-trifluoromethyl pyrazol-4-yl)-3-oxyethyl group methoxy base vinyl cyanide (compound V-44):
0.6g 2-(uncle 2-Ding Ji oxazole-4-yl)-3-(5-chloro-3-Trifluoromethyl-1-methyl-pyrazoles-4-yl)-3-hydroxyl vinyl cyanide is dissolved in 5ml THF; And under with ice-cooled situation, add 0.07g 60% sodium hydride; Then, at room temperature, stirred 15 minutes.0.17g ethoxyl methyl chlorine is added wherein, and at room temperature, stirred 6 days.Pour reaction mixture into frozen water, use ethyl acetate extraction, and wash with saturated brine.With the product anhydrous sodium sulfate drying that generates, and removing solvent under reduced pressure. the residual product that is generated is passed through silica gel thin-layer chromatography, and (ethyl acetate: purifying normal hexane=1: 4) obtains the purpose compound that 0.1g exists with vitreousness.
1H-NMR(CDCl 3，δppm)；1.17(3H，t)，1.41(9H，s)，
3.98(3H，s)，5.03(2H，s)，8.00(1H，s)
[synthetic embodiment 11]
Synthesizing of 2-phenyl-3-(3,5-two chloro-1-methyl-pyrazol-4-yls)-acrolactic acid ethyl ester (compound IV-91):
With 8.2g (50mmol) Phenylacetic acid ethylester and 10.7g (50mmol) 3,5-two chloro-1-methylpyrazole-4-formyl chlorides are dissolved in the 100ml anhydrous tetrahydro furan, and at room temperature, add 14g (125mmol) potassium tert.-butoxide.At room temperature, stirred this reaction mixture 1 hour, add 300ml water again, and use ethyl acetate extraction.After organic layer water and saturated brine washing, use anhydrous magnesium sulfate drying, remove solvent again under reduced pressure, obtain 17g object 2-phenyl-3-(3,5-two chloro-1-methyl-pyrazol-4-yls)-acrolactic acid ethyl ester.
1H-NMR(CDCl 3，δppm)；1.1-1.5(3H，m)，3.59(1.5H，s)，
3.73(1.5H，s)，3.95-4.45(2H，m)，
5.58(0.5H，s)，7.0-7.35(5H，m)，
13.21(0.5H，s)
[synthetic embodiment 12]
Synthesizing of 1-(3,5-two chloro-1-methyl-pyrazol-4-yls)-2-phenyl-2-bromine ethyl ketone (compound IV-90):
1) 17g (50mmol) 2-phenyl-3-(3,5-two chloro-1-methyl-pyrazol-4-yls)-acrolactic acid ethyl ester is dissolved in 50ml 6N HCl and 250ml 1, in the 4-diox, and under the backflow situation, heated 15 hours.Pour reaction mixture into the 500ml frozen water, the crystal that is settled out is come out by filtering separation, obtain 8g object 1-(3,5-two chloro-1-methyl-pyrazol-4-yls)-2-phenyl ethyl ketone white crystal.m.p.：94-96℃
2) 5.38g (20mmol) 1-(3,5-two chloro-1-methyl-pyrazol-4-yls)-2-diphenylphosphino ethane is dissolved in the 50ml chloroform, and at room temperature, stirred 1 hour; Then, remove solvent under reduced pressure, obtain object 1-(3,5-two chloro-1-methyl-pyrazol-4-yls)-2-bromo phenyl ethyl ketone white crystal.m.p.：74.5-75.5℃
[synthetic embodiment 13]
Synthesizing of 1-(3,5-two chloro-1-methyl-pyrazol-4-yls)-1-new pentane acyloxy-2-phenyl-2-bromine ethene (compound IV-92):
0.55g (1.58mmol) 1-(3,5-two chloro-1-methyl-pyrazol-4-yls)-2-phenyl-monobromethane and 0.18g (1.74mmol) triethylamine are dissolved in the 4ml anhydrous tetrahydro furan, and at room temperature, add 0.19g (1.58mmol) pivalyl chloride.At room temperature, the reaction mixture stirring after 16 hours, is added 10ml water wherein, and uses ethyl acetate extraction.After organic layer water and saturated brine washing, use anhydrous magnesium sulfate drying, remove solvent again under reduced pressure.The gained resistates by purification by silica gel column chromatography, is obtained 0.23g object 1-(3,5-two chloro-1-methyl-pyrazol-4-yls)-1-new pentane acyloxy-2-phenyl-2-bromine ethene colourless liquid (E-Z mixture).
1H-NMR(CDCl 3，δppm)；1.05(9H，s)，3.81(3H，s)，
7.37 (5H, m): main component
1.32(9H，s)，3.62(3H，s)，
7.24 (5H, m): submember
[synthetic embodiment 14]
1-(3,5-two chloro-1-methyl-pyrazol-4-yls)-2-{2-(1-methyl cyclohexane-1-yl)-thiazole-4-yl } 2-diethyl phosphonyl ethyl ketone (Compound I I-156) synthetic:
1) 4.15g (18.1mmol) 2-(1-methyl-cyclohexyl-1-yl)-4-5-chloromethyl thiazole and 3.32g (20mmol) trimethyl phosphite are mixed, and under situation about refluxing, heated 16 hours.Reaction mixture is cooled to room temperature, and obtains 4.63g object { 2-(1-methyl cyclohexane-1-yl)-thiazole-4-yl } methyl-phosphorous acid diethyl ester colourless liquid by purification by silica gel column chromatography.
1H-NMR(CDCl 3，δppm)；1.25(3H，t，J＝7.2Hz)，1.31(3H，s)，
1.1-2.3(10H，m)，
3.33(2H，d，J＝20.4Hz)，
4.04(4H，dd，J＝7.2，7.2Hz)，
7.01(1H，m)
2) with 0.85g (4mmol) 3,5-two chloro-1-methylpyrazole-4-formyl chlorides and 1.32g (4mmol) { 2-(1-methyl cyclohexane-1-yl)-thiazole-4-yl } methyl-phosphorous acid diethyl ester is dissolved in the 15ml anhydrous tetrahydro furan, and at room temperature, add 1.12g (10mmol) potassium tert.-butoxide.At room temperature, stirred reaction mixture 1 hour adds 20ml water, and uses ethyl acetate extraction.After organic layer water and saturated brine washing, use anhydrous magnesium sulfate drying, remove solvent again under reduced pressure.The gained resistates by purification by silica gel column chromatography, is obtained 0.4g object 1-(3,5-two chloro-1-methyl-pyrazol-4-yls)-2-{2-(1-methyl cyclohexane-1-yl)-thiazole-4-yl }-2-diethyl phosphonyl ethyl ketone.
1H-NMR(CDCl 3，δppm)；1.23(3H，t，J＝7.2Hz)，1.23(3H，s)，
1.1-2.3(10H，m)，3.79(3H，s)，
4.09(2H，dd，J＝7.2，7.2Hz)，
5.90(1H，d，J＝22.8Hz)，7.43(1H，m)
[synthetic embodiment 15]
2-{3-(2, the 6-difluorophenyl) pyrazol-1-yl }-3-(5-chloro-1-methyl-3-trifluoromethyl pyrazol-4-yl)-acrolactic acid allyl ester (Compound I-133) synthetic:
1) salt of wormwood (1.53g) is added in acetonitrile (10ml) solution of 3-(2, the 6-difluorophenyl) pyrazoles (1g) and 2-bromoacetic acid allyl ester (1.49g), and refluxed 3 hours.At room temperature, the product that generates is extracted with the ethyl acetate and the dilute hydrochloric acid that add wherein.Organic layer is used anhydrous magnesium sulfate drying and concentrated, and the enriched material that obtains is obtained 2-{3-(2, the 6-difluorophenyl) pyrazol-1-yl by silica gel column chromatography (chloroform) allyl acetate (1.5g).
1H-NMR(CDCl 3，δppm)；4.70(2H，d，J＝6.0Hz)，5.10(2H，s)，
5.30-5.60(2H，m)，5.70-6.40(1H，m)，
6.50-7.80(5H，m)
2) under 0 ℃, potassium tert.-butoxide (0.5g) is added by 2-{3-(2, the 6-difluorophenyl) pyrazol-1-yl } allyl acetate (0.5g) and 5-chloro-1-methyl-3-trifluoromethyl pyrazol-4-formyl chloride (0.44g) in THF (10ml) in the formed solution, and stirred 5 minutes.Water (5ml) is added wherein, then, with dilute hydrochloric acid and ethyl acetate extraction.With organic layer with anhydrous magnesium sulfate drying after, concentrate, and with the enriched material that obtains by silica gel column chromatography (chloroform) purifying, obtain the purpose product: Compound I-133 (0.89g).
1H-NMR(CDCl 3，δppm)：3.95(3H，s)，4.80(2H，d，J＝6.0Hz)，
5.20-5.60(2H，m)，5.60-6.40(1H，m)，
6.45-7.90(6H，m)
[synthetic embodiment 16]
2-bromo-2-{3-(2, the 6-difluorophenyl) pyrazol-1-yl }-1-(5-chloro-1-methyl-3-trifluoromethyl pyrazol-4-yl)-1-hydroxyl ethene (Compound I-134) synthetic:
1) at room temperature, in nitrogen atmosphere, formic acid (60mg) is added in THF (1ml) solution of acid chloride (7mg) and triphenyl phosphine (17mg).THF (5ml) solution of Compound I-133 (0.32g) is added wherein, and refluxed 1 hour.Reaction mixture is at room temperature left standstill, concentrate, again the gained enriched material is passed through silica gel column chromatography (chloroform) purifying, and recrystallization (chloroform-diisopropyl ether) obtains 2-{3-(2, the 6-difluorophenyl) pyrazol-1-yl }-3-(5-chloro-1-methyl-3-trifluoromethyl pyrazol-4-yl) second-1-ketone (0.1g).m.p.：152-154℃
2) under-78 ℃, the THF solution (0.27ml) of 1M hexamethyldisilane yl amino lithium (lithiumhexamethyldisilazide) is added 2-{3-(2, the 6-difluorophenyl) pyrazol-1-yl }-the THF solution of 3-(5-chloro-1-methyl-3-trifluoromethyl pyrazol-4-yl) second-1-ketone (0.1g) in, and under same temperature, in nitrogen atmosphere, stir.In the solution that generates, add THF (2ml) solution of carbon tetrabromide (0.098g), then, be heated to room temperature gradually.Water (1ml) is added wherein, use dilute hydrochloric acid and ethyl acetate extraction then.With the organic layer anhydrous magnesium sulfate drying, concentrate, and recrystallization obtains the purpose product from chloroform-ether: Compound I-134 (0.062g).m.p.：123-125℃
[synthetic embodiment 17]
2-bromo-2-{3-(2, the 6-difluorophenyl) pyrazol-1-yl }-1-(5-chloro-1-methyl-3-trifluoromethyl pyrazol-4-yl)-1-new pentane acyloxy ethene (Compound I-135) synthetic:
Under 0 ℃, successively triethylamine (0.3g) and pivalyl chloride (0.23g) are added chloroform (25ml) solution of Compound I-134 (0.47g), and at room temperature stirred 1 hour.With products therefrom water and chloroform extraction.With organic layer with anhydrous magnesium sulfate drying after, concentrate, and, obtain the purpose product: Compound I-135 (0.4g) by silica gel column chromatography (chloroform) purifying.
1H-NMR(CDCl 3，δppm)；1.25(9H，s)，3.90(3H，s)，
6.55-7.80(5H，m)
According to above-mentioned reaction process and embodiment, can make various The compounds of this invention, the structure of this compound and fusing point are shown in table 15 hereinafter to table 19.Unless otherwise indicated, otherwise the compound shown in the table is a form of mixtures with E-type and Z-type exists. the implication of abridging in the table is the same.
Table 15
No. R 1 R 2 R 3 E B A m.p.(℃)
I-1 I-2 I-3 I-4 I-5 I-6 I-7 I-8 I-9 I-10 I-11 I-12 I-13 I-14 I-15 I-16 I-17 I-18 I-19 I-20 I-21 I-22 I-23 Ph Ph Ph Ph Ph Ph Ph Ph Ph Ph 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals H Cl H Me H H CO 2Et H H H H H H H H H H H H H H H H H H Me H H H H H H H H H H H H H H H H H H H H CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN H H H H B1 B2 H H H H H H H H H H H H H H H H B7 A1 A1 A1 A1 A1 A1 A1 A2 A7 A8 A1 A2 A3 A4 A6 A7 A8 A9 A10 A11 A12 A13 A7 144-145 300＜ 300＜ 141-143 75-77 *Viscous oil 202-203 300＜124-125 265-267 290＜300＜260-267 300＜297-298 163-165 300＜240-245 261-266 232-234 284-287 300＜103-110*
Table 15 (continuing)
No. R 1 R 2 R 3 E B A m.p.(℃)
I-24 I-25 I-26 I-27 I-28 I-29 I-30 I-31 I-32 I-33 I-34 I-35 I-36 I-37 I-38 I-39 I-40 I-41 I-42 I-43 I-44 I-45 I-46 2-pyridine radicals 3-pyridine radicals 3-pyridine radicals 3-pyridine radicals 4-pyridine radicals 2-F-Ph 2-F-Ph 2-F-Ph 3-F-Ph 4-F-Ph 2-Cl-Ph 2-Cl-Ph 3-Cl-Ph 3-Cl-Ph 4-Cl-Ph 4-Cl-Ph 2,6-F2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-Cl 2-Ph 2，6-Cl 2-Ph tBu tBu H H H H H H H Cl H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN B8 H H H H H H H H H H H H H H H H H H H H H H A1 A1 A2 A7 A1 A1 A2 A1 A2 A2 A1 A2 A1 A7 A1 A7 A1 A2 A7 A1 A2 A1 A2 Viscous oil 298-300 158-160 168-169 251-253 125-126 281-282 281-287 300＜169-173 viscous oil viscous oil 141-149 291-293 186-188 300＜267-269 300＜242-243 147-148 100-102 viscous oil 65-67
Table 15 (continuing)
No. R 1 R 2 R 3 E B A m.p.(℃)
I-47 I-48 I-49 I-50 I-51 I-52 I-53 I-54 I-55 I-56 I-57 I-58 I-59 I-60 I-61 I-62 I-63 I-64 I-65 I-66 I-67 I-68 I-69 2-MeO-Ph 2-MeO-Ph H Me cHex 1-naphthyl 2-thienyl 2-thienyl Ph Ph Ph Ph Ph tBu tBu Ph 2,6-F2-Ph Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2-pyridyl H H CO 2Et Ph H H H H H H H H H CO 2Me CO 2Me H H H H H H H H H H Ph H H H H H H H H H H H H H H H H H H H H CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN H H H H H H H H H B1 B7 B8 CO 2 tBu H B7 B7 B8 B6 Na Na Na H B8 A1 A2 A1 A1 A1 A1 A1 A7 A34 A34 A1 A1 A1 A1 A1 A2 A2 A2 2，6-(MeO) 2-Ph 2-CF 3O-Ph 2-MeO-Ph 2-CF 3O-Ph A7 300＜300＜236-237 viscous oil 204-205 225-227 146-147 271-273 173.3-174.1 viscous oil* 140-141 * 50-51 *Viscous oil 105-106 125-126 viscous oil 200-201 viscous oil 300＜282.8-287.2 300＜157.9-160.1 118-119*
Table 15 (continuing)
No. R 1 R 2 R 3 E B A m.p.(℃)
I-70 I-71 I-72 I-73 I-74 I-75 I-76 I-77 I-78 I-79 I-80 I-81 I-82 I-83 I-84 I-85 I-86 I-87 I-88 I-89 I-90 I-91 I-92 2，6-F 2-Ph Ph Ph Ph Ph Ph Ph Ph Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals H H H H H H Ph H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN B7 H H H H H H H B35 H H H H H H H H H H B7 Na H CO nC 17H 35 A2 2-Cl-Ph 2，6-F 2-Ph 2，6-Cl 2-Ph 2-CF 3-Ph 1-naphthyl A2 2-Cl-4-F-Ph A2 2-Me-Ph 2-Cl-6-F-Ph 2-NO2-Ph 2-AcO-Ph 2.6-Me-Ph 2，6-F 2-Ph 2，6-Cl 2-Ph 2-NO 2-Ph 2-MeO-Ph 2-CO 2Me-Ph 2-Cl-Ph 2-Cl-Ph pyridine-2-base A7 Viscous oil 108-109 167-168 170-171 viscous oil 137-138 145-147 94-95 164-165 113.1-119.8 144-146 176-179 vitreousness vitreousness 188-189 278-280 285-287 275-276 248-249 124-125 278-280 216-217 58-59
Table 15 (continuing)
No. R 1 R 2 R 3 E B A m.p.(℃)
I-93 I-94 I-95 I-96 I-97 I-98 I-99 I-100 I-101 I-102 I-103 I-104 I-105 I-106 I-107 I-108 I-109 I-110 I-111 I-112 I-113 I-114 I-115 t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu CO 2Me CO 2Me CO 2Me H H NO 2 Br CN CN CN CN Cl CO 2Me Cl NO 2 CO 2 nHex CO 2Me Me CO 2Me CO 2Me CO 2Me Me CO 2Me H H H H H H H H H H H H H H H H H H H H H H H CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN H B7 H B7 B7 B7 B7 H CO 2 tBu CO 2 tBu CO 2Ph B7 CO 2 iBu H H H B8 H CO nC 17H 35 B7 H B7 B7 2-Cl-4-F-Ph A2 A2 A2 A2 A2 A2 A2 A2 A2 A2 A2 A2 A2 A2 A2 A2 A2 A14 A14 A14 A2 A3 114-115 105-106 102-103 viscous oil viscous oil #1Viscous oil viscous oil 178-180 vitreousness 201-202.5 #2Vitreousness viscous oil 155.8-156.9 viscous oil 87-88 vitreousness 152.1-153.5 vitreousness viscous oil viscous oil 101-102 vitreousness 131-132
Table 15 (continuing)
No. R 1 R 2 R 3 E B A m.p.(℃)
I-116 I-117 I-118 I-119 I-120 I-121 I-122 I-123 I-124 I-125 I-126 I-127 I-128 I-129 I-130 I-131 I-132 I-133 I-134 I-135 I-136 I-137 I-138 t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu H H H H Ph Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2-pyridyl 2-pyridyl 2-pyridyl CO 2Me CO 2Me CO 2Me CO 2Me CO 2Me CO 2Me CO 2Me CO 2Me CO 2Me H Ph t-Bu t-Bu H H H H H H H H H Cl H H H H H H H H H 2，6-F 2-Ph H H H H H H H H H H H H H CN CN CN CN CN CN CN CN CN CN CN CN CN CO 2Me CO 2Me CO 2Me COMe CO 2CH 2CH＝CH 2 Br Br CN CN CN Me B3 H CO nC 9H 19 B7 H B7 CO nC 5H 11 CO nC 5H 11 H H B7 H H B7 H H H H B7 B7 B7 B7 A2 A14 A21 A3 A15 A15 A21 A21 A21 A2 A1 A2 A2 A1 A2 A2 A2 A2 A2 A2 A37 A10 A7 166-167 *Viscous oil 152.6-154 viscous oil 125-127 *138-139 viscous oil viscous oil viscous oil #3157.4-162.4 vitreousness vitreousness vitreousness 158-160 viscous oil 248-250 vitreousness vitreousness 123-125 vitreousness 86-94#492-93 viscous oil *
*: E-type or Z-type
The geometrical isomer of #1:I-96
The geometrical isomer of #2:I-101
The geometrical isomer of #3:I-123
#4:E/Z=2/1 and mixture
Table 16
Figure C9719404103341
No. R E B A m.p.(℃)
II-1 II-2 II-3 II-4 II-5 II-6 II-7 II-8 II-9 II-10 II-11 II-12 II-13 II-14 II-15 II-16 II-17 II-18 II-19 II-20 II-21 II-22 II-23 Ph 2-Cl-Ph t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu 2-pyridine radicals CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN H H H B3 B7 H B7 H H B6 B5 B8 SO 2(4-Cl-Ph) H H H B7 CO 2Et CO 2CH 2Ph CONMe 2 CH 2CO 2Me PO(OEt) 2 H A1 A2 A2 A2 A2 A1 A1 2，6-F 2-Ph 2-Cl-Ph A2 A2 A2 A2 2，6-Cl 2-Ph 2-CF 3-Ph A3 A3 A2 A2 A2 A2 A2 A2 200-205 137-138 151-153 147-150 * 89.5-92 *Viscous oil *Viscous oil *90-92.5 96.2-98.6 vitreousness *Viscous oil viscous oil vitreousness *150.3-151.7 71.9-79.6 viscous oil viscous oil *Viscous oil viscous oil 136.7-138.2 viscous oil viscous oil 184.5-188.5
Table 16 (continuing)
No. R E B A m.p.(℃)
II-24 II-25 II-26 II-27 II-28 II-29 II-30 II-31 II-32 II-33 II-34 II-35 II-36 II-37 II-38 II-39 II-40 II-41 II-42 II-43 II-44 II-45 II-46 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals c-Hex c-Hex c-Hex c-Hex 2,6-F2-Ph 2，6-F 2-Ph 2-Cl-Ph t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN H B7 B7 H B7 H B7 H B7 H H B7 B7 H B7 H B35 B35 B36 H B28 B30 B30 A7 A7 A2 A3 A3 A35 A35 A36 A36 A2 2，6-F 2-Ph 2，6-F 2-Ph A2 A2 A2 A2 A2 A2 A2 A13 A2 A2 A2 210.3-218.8 162.7-167 *Vitreousness *The 148-151 vitreousness * 188-193 200.5-202.5 *Viscous oil viscous oil 126.5-128.1 110.9-112.7 111.2-117.4 *Viscous oil * 176.8-178.2 95.9-98.0 *172.9-175.2 vitreousness vitreousness #4Vitreousness 168-173 vitreousness vitreousness vitreousness #5
Table 16 (continuing)
No. R E B A m.p.(℃)
II-47 II-48 II-49 II-50 II-51 II-52 II-53 II-54 II-55 II-56 II-57 II-58 II-59 II-60 II-61 II-62 II-63 II-64 II-65 II-66 II-67 II-68 II-69 t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CO (2-Me-Ph) B38 B37 nicotinoyl B40 CO 2 iBu CO 2Ph B41 CO 2 nHex H H H H H CO(2-MeS-Ph) H H B7 B15 B38 B39 CO(4-Cl-Ph) CO(3-Cl-Ph) A2 A2 A2 A2 A2 A2 A2 A2 A2 3-Cl-Ph 3-F-Ph 2-Br-Ph 2-I-Ph 2-Cl-6-F-Ph A2 2-MeS-Ph A22 A22 A22 A13 A2 A2 A2 Vitreousness vitreousness vitreousness vitreousness vitreousness viscous oil viscous oil viscous oil viscous oil 89.7-91.1 63.7-64.4 86-87 vitreousness 109.6-110.6 vitreousness 120.6-122.1 113-118 98-99.5*Viscous oil viscous oil vitreousness vitreousness vitreousness
Table 16 (continuing)
No. R E B A m.p.(℃)
II-70 II-71 II-72 II-73 II-74 II-75 II-76 II-77 II-78 II-79 II-80 II-81 II-82 II-83 II-84 II-85 II-86 II-87 II-88 II-89 II-90 II-91 II-92 t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN B7 B8 B6 CO 2 nPr CO 2 nBu B6 CO 2CH 2CCl 3 CO(2-Cl-Ph) CO(3-CF 3-Ph) CO(4-CF 3-Ph) CO(3-NO 2-Ph) CO(2-Cl-6-F-Ph) CO 2 cPen 3-Cl-valeryl CO 2 iPr CO 2CH 2CH 2Cl CO 2CHClCH 3 CO iThe different nicotinoyl picoline of Pr acyl group CO (4-Me-Ph) CO (4-NO 2-Ph) methacryloyl 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph A2 A2 A13 A2 A2 A2 A2 A2 A2 2，6-F 2-Ph A2 A2 A2 A2 A2 A2 A2 A2 A2 A2 Viscous oil viscous oil 150.2-151.3 viscous oil viscous oil viscous oil viscous oil vitreousness vitreousness vitreousness vitreousness vitreousness vitreousness viscous oil*Viscous oil viscous oil viscous oil viscous oil viscous oil viscous oil viscous oil viscous oil viscous oil
Table 16 (continuing)
No. R E B A m.p.(℃)
II-93 II-94 II-95 II-96 II-97 II-98 II-99 II-100 II-101 II-102 II-103 II-104 II-105 II-106 II-107 II-108 II-109 II-110 II-111 II-112 II-113 II-114 II-115 t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN B15 PhCH 2 Me CBrF 2 CO nPr CO iBu B43 PhCOCH 2B42 H H B7 cinnamoyl H B7 B7 B7 COnC 17H 35 PhCH 2CO B7 H H CO 2 iBu A2 A2 A2 A2 A2 A2 A2 A2 A2 A14 A16 A16 A2 A23 A23 A14 A14 A14 A2 A17 A17 A24 A24 Vitreousness viscous oil 136.5-138 84-86.5 viscous oil viscous oil vitreousness 148-152* 128-129.5 *98-99 viscous oil viscous oil *Vitreousness 109-112 120-122.5 viscous oil viscous oil #6Viscous oil viscous oil viscous oil 140-143 115-117 vitreousness
Table 16 (continuing)
No. R E B A m.p.(℃)
II-116 II-117 II-118 II-119 II-120 II-121 II-122 II-123 II-124 II-125 II-126 II-127 II-128 II-129 II-130 II-131 II-132 II-133 II-134 II-135 II-136 II-137 II-138 t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu 2，6-F 2-Ph 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN B7 H B7 H CO 2(4-Me-Ph) H B7 H H H B8 B8 H H H B7 H H B7 H H CO 2(4-F-Ph) H A2 A25 A25 A31 A31 A26 A26 A27 A28 A29 A29 A29 A32 A33 2，6-F 2-Ph A18 A18 A9 A9 A8 A10 A10 A24 69.5-73.5 #7107-109 viscous oil 116-117 92-93 133.2-135.4 133.9-145 46-47 168-169 94.7-95.4 viscous oil viscous oil#8 133.9-134.4 220-230 138-143 115-145 176-178 191.5-195 101-103 211-216 189-193 137-142 188-191.5
Table 16 (continuing)
No. R E B A m.p.(℃)
II-139 II-140 II-141 II-142 II-143 II-144 II-145 II-146 II-147 II-148 II-149 II-150 II-151 II-152 II-153 II-154 II-155 II-156 II-157 II-158 II-159 II-160 II-161 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals 2-pyridine radicals NMePh NMePh NMePh NMePh 1-piperidyl 1-piperidyl 1-piperidyl 1-piperidyl 1-piperidyl 1-piperidyl 1-naphthyl 1-naphthyl t-Bu 1-Me-1-cHex t-Bu t-Bu 1-Me-1- cHex n-Pen t-Bu CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CO 2Me PO(OEt) 2 CO 2Et CO 2Et CN CN CN B7 B7 H H H B7 H B7 B3 H H B8 B8 B6 H B7 H H H B7 H H B8 A24 A30 A30 A13 A7 A7 A2 A2 A2 A2 A7 A7 A2 A2 A2 A2 A2 A1 A1 A1 A2 A2 A32 160-163.5 123-125 165-166 149.5-151 161.5-164 120-123 vitreousness vitreousness 165.5-169 151-153 187-190 viscous oil 120-121.5 viscous oil 161-163 vitreousness viscous oil vitreousness viscous oil viscous oil vitreousness 73-75 108-112
Table 16 (continuing)
No. R E B A m.p.(℃)
II-162 II-163 II-164 II-165 II-166 II-167 II-168 II-169 II-170 II-171 II-172 II-173 II-174 II-175 II-176 II-177 II-178 II-179 t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu 1-Me-1- cHex n-Pen 1-Me-1- cHex t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu CN CO 2Me SO 2Ph SO 2Ph SO 2Ph CO 2Me CO 2Me CO 2CH 2CH＝CH 2 CO 2CH 2CH＝CH 2CN CN CN 5-Me-1,3,4-oxadiazole-2-base 5-Me-1,3,4-oxadiazole-2-base Bu CN 5-Me-1,3,4-oxadiazole-2-base 5-Me-1,3,4-oxadiazole-2-base H H H B7 B7 B7 B7 H B7 B7 B7 CH 2O(CH 2) 2OCH 3 H H H B6 B7 B7 A1 A1 A1 A1 A1 A1 A2 A2 A2 A2 A2 A2 A1 A1 A2 A13 A1 A1 Viscous oil 89-92 145-148 122-123 152-153 #14Viscous oil 76-78 viscous oil viscous oil vitreousness vitreousness 97-98 *Vitreousness vitreousness viscous oil 104-107 * 134-137 114-116 #15
Table 16 (continuing)
No. R E B A m.p.(℃)
II-180 t-Bu 5-Me-1,3,4-thiadiazoles-2-base B7 A1 86-90 *
*: E-type or Z-type
The geometrical isomer of #4:II-40
The geometrical isomer of #5:II-45
The geometrical isomer of #6:II-108
The geometrical isomer of #7:II-5
The geometrical isomer of #8:II-126
The geometrical isomer of #14:II-165
The geometrical isomer of #15:II-178
Table 17
Figure C9719404103431
No. R E B A m.p.(℃)
III-1 III-2 III-3 III-4 III-5 III-6 III-7 III-8 III-9 III-10 III-11 III-12 III-13 III-14 III-15 III-16 III-17 III-18 III-19 III-20 III-21 Ph Ph t-Bu t-Bu t-Bu t-Bu 2-amyl group 4-tBu-Ph t-Bu t-Bu t-Bu t-Bu 2-NO 2-Ph 1-naphthyl t-Bu Ph t-Bu 2-Cl-6-F-Ph 2,6-F 2-Ph Ph Ph CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN B4 B5 B1 B4 B6 B7 B1 B1 Na B9 B10 B11 B9 B9 B7 B4 B4 B7 B7 B5 B7 A1 A1 A1 A1 A2 A2 A1 A5 A2 A2 A2 A2 A1 A7 A2 A1 A1 A2 A2 A1 A2 Viscous oil * 40-41 * 151-152 * 77-79 * 55-61 *Viscous oil *Viscous oil viscous oil 165-174 viscous oil 185-186 *Viscous oil 168-171 * 136-138 *Viscous oil #9Solid #10Viscous oil #11The 152-153 vitreousness * 105-107 #12Viscous oil
*: the geometrical isomer of E-type or Z-type #9:III-6, the geometrical isomer of #10:III-1, the geometrical isomer of #11:III-4, the rotamerism body surface 18 of #12:III-2
No. G E B A m.p.(℃)
IV-1 IV-2 IV-3 IV-4 IV-5 IV-6 IV-7 IV-8 IV-9 IV-10 IV-11 IV-12 IV-13 IV-14 IV-15 IV-16 IV-17 IV-18 IV-19 IV-20 IV-21 IV-22 IV-23 2-CF 3 3-CF 3 3-CF 3 4-CF 3 4-CF 3 2-CF 3 3(1-CN-1-Me)-Et 3(1-CN-1-Me)-Et 3-OPh 3-OPh 4-OPh 4-OPh 4-Et 4-Et 4-Et 4-i-Pr 4-i-Pr 4-t-Bu 4-t-Bu 4-OCF 3 4-OCF 33,4-methylene-dioxy 3,4-methylene-dioxy CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN H H B1 H B1 CSNMe 2 H B1 H B7 H B7 H B7 B5 H B7 H B1 H B7 H B7 A1 A1 A1 A1 A1 A1 A1 A1 A1 A1 A1 A1 A1 A1 A1 A1 A1 A1 A1 A1 A1 A1 A1 Viscous oil 159-163 174-175 176-179 viscous oil viscous oil viscous oil 148-155 103-110 viscous oil 148-150 viscous oil 148-149 81-82 viscous oil 126-127 105-106 117-118 viscous oil 128-129 96-99 129-131 viscous oil
Table 18 (continuing)
No. G E B A m.p.(℃)
IV-24 IV-25 IV-26 IV-27 IV-28 IV-29 IV-30 IV-31 IV-32 IV-33 IV-34 IV-35 IV-36 IV-37 IV-38 IV-39 IV-40 IV-41 IV-42 IV-43 IV-44 IV-45 IV-46 4-t-Bu 4-t-Bu 4-t-Bu 4-t-Bu 4-t-Bu 4-t-Bu 4-t-Bu 4-t-Bu 4-t-Bu 4-t-Bu 4-t-Bu 4-t-Bu 4-t-Bu 4-t-Bu 4-t-Bu 4-t-Bu 4-t-Bu 4-t-Bu 4-s-Bu 4-s-Bu 4-i-Pr 4-i-Pr 4-i-Pr CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN B7 B15 H B7 H B8 H H B7 B15 B7 B7 B8 H B8 CO 2Et CO 2 iBu COCO 2CH 3 H B15 B15 B15 H A2 A2 A2 A13 A13 A2 A19 A20 A20 A14 A19 A1 A1 A24 A24 A1 A1 A1 A2 A2 A1 A2 A2 Viscous oil viscous oil 139-140 87-88 141-142 vitreousness 169.5-173 vitreousness 146-148 viscous oil vitreousness viscous oil viscous oil vitreousness vitreousness viscous oil viscous oil viscous oil 107-108 77-85 100-101 viscous oil 98-99
Table 18 (continuing)
No. G E B A m.p.(℃)
IV-47 IV-48 IV-49 IV-50 IV-51 IV-52 IV-53 IV-54 IV-55 IV-56 IV-57 IV-58 IV-59 IV-60 IV-61 IV-62 IV-63 IV-64 IV-65 IV-66 IV-67 IV-68 IV-69 4-i-Pr 4-i-Pr 4-Et 4-Ph 4-Ph 4-Ph 4-Ph 3，4-Cl 2 4-Cl 2-F-4-CF 3 2-F-4-CF 3 2-F-4-CF 3 4-NO 2 4-MeO 4-MeO 4-i-PrO 4-i-PrO 4-i-PrO 4-i-PrO 4-i-PrO 4-n-BuO 4-n-BuO 4-n-BuO CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN B8 CO(4-NO 2-Ph) B15 H H H H H H H B7 B15 H H B15 H H B15 B15 B6 H B15 H A2 A2 A1 A1 A2 A12 A13 A1 A1 A2 A2 A2 A1 A1 A1 A1 A2 A1 A2 A2 A1 A1 A2 Viscous oil vitreousness viscous oil vitreousness vitreousness vitreousness 167-169 vitreousness vitreousness vitreousness vitreousness vitreousness 186-188 108-110 viscous oil*127-131 141.4-148.3 viscous oil viscous oil viscous oil 101-104 75-70 104.6-105.4
Table 18 (continuing)
No. G E B A m.p.(℃)
IV-70 IV-71 IV-72 IV-73 IV-74 IV-75 IV-76 IV-77 IV-78 IV-79 IV-80 IV-81 IV-82 IV-83 IV-84 IV-85 IV-86 IV-87 IV-88 IV-89 IV-90 IV-91 IV-92 4-n-BuO 4-n-BuO 4-tert-pentyl 4-allyloxy 4-allyloxy 4-(Cl 2C＝CHCH 2O) 4-(Cl 2C＝CHCH 2O) 4-(ClCCCH 2O) 4-PhCH 2O 4-PhCH 2O 4-PhCH 2O 4-MeOCH 2O 4-CF 3CH 2O 4-valeryl 4-valeryl 4-Me 2NCO 2 4-Me 2NCO 2 4-Me 2NCO 2 4-t-Bu 4-t-Bu H H H CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN PO(OEt) 2 PO(OEt) 2 Br CO 2Et Br B8 B15 B15 H B15 H B15 H H H B15 H H B15 H H B15 B7 H B1 H H B7 A1 A2 A2 A1 A1 A1 A1 A1 A1 A2 A2 A1 A1 A2 A2 A2 A2 A2 A1 A1 A1 A1 A1 77.1-80.7 viscous oil viscous oil vitreousness vitreousness vitreousness vitreousness vitreousness 152.9-154.7 189-190.5 123-129 130.4-131.7 100-103 vitreousness vitreousness vitreousness vitreousness vitreousness 87-88 121-124 74.5-75.5 viscous oil viscous oil
Table 18 (continuing)
No. G E B A m.p.(℃)
IV-93 IV-94 IV-95 IV-96 IV-97 IV-98 IV-99 IV-100 IV-101 IV-102 IV-103 IV-104 IV-105 IV-106 IV-107 IV-108 IV-109 IV-110 IV-111 IV-112 IV-113 IV-114 IV-115 4-t-Bu 4-t-Bu 4-t-Bu 4-t-Bu 4-t-Bu H 4-t-Bu 4-t-Bu 4-t-Bu 4-t-Bu 4-t-Bu 4-t-Bu 4-t-Bu 4-t-Bu 4-t-Bu 4-t-Bu 4-t-Bu 4-CHF 2O 4-CHF 2O 4-CHF 2O 4-CH 3CONH 4-CH 3CONH 4-CO 2Me PO(OEt) 2 CN CN CN SO 2Ph CO 2Et CN CN CN CN CO 2Me CO 2Me CO 2Me CO 2Me SO 2Ph SO 2Ph CN CN CN CN CN CN CN H COCO 2Et CO 2 iBu CO 2 iBu H B7 B3 B19 CO(4-CO 2Me-Ph) CO(4-CO 2Me-Ph) H H B7 B7 B7 B7 B3 H B15 B7 H B7 H A2 A1 A2 A13 A1 A1 A1 A1 A2 A13 A2 A1 A1 A2 A1 A1 A2 A2 A2 A2 A2 A2 A2 Viscous oil viscous oil viscous oil 104-105 143-145 viscous oil viscous oil vitreousness vitreousness vitreousness 88-89 123-124 77-78 viscous oil 98-99 130-131#13 71-72 *Vitreousness vitreousness vitreousness 247.9-251.9 82.1-84.3 151-152
Table 18 (continuing)
No. G E B A m.p.(℃)
IV-116 IV-117 IV-118 IV-119 IV-120 IV-121 IV-122 IV-123 IV-124 IV-125 IV-126 IV-127 IV-128 IV-129 IV-130 IV-131 IV-132 IV-133 IV-134 IV-135 IV-136 IV-137 IV-138 4-CO 2Me 4-vinyl 4-t-Bu 4-t-Bu 4-t-Bu 4-t-Bu 4-t-Bu 4-t-Bu H 4-t-Bu 4-SMe 4-SMe 4-SOMe 4-t-Bu 4-t-Bu 4-t-Bu 4-t-Bu 4-t-Bu 4-SO 2Me 4-SOMe 4-OCH 2Ph-3-Cl 4-OPr i-3-Cl 4-OBu i-3-Cl CN CN CN CN CN CN CN CN Cl 5-Me-1; 3,4-oxadiazole-2-base CN CN CN CN CN CN CN CN CN CN CN CN CN B7 H B15 methacryloyl COCH=(CH 3) 2 B33 CH 2OCH 2Ph B24 H H H B7 H B33 B3 B7 B3 COCH 2(4-OMe-Ph) B7 B7 H H H A2 A2 A1 A1 A1 A1 A1 A1 A1 A1 A2 A2 A2 A2 A13 A3 A3 A1 A2 A2 A2 A2 A2 Viscous oil *Vitreousness 78-82 viscous oil *Viscous oil viscous oil viscous oil viscous oil 48-49 149-151 154-156 viscous oil*Vitreousness viscous oil 111-112 *Viscous oil viscous oil 117-121 vitreousness *Vitreousness *Vitreousness vitreousness vitreousness
Table 18 (continuing)
No. G E B A m.p.(℃)
IV-139 IV-140 4-t-Bu 4-t-Bu CN CN B8 B7 A3 2-Cl-4-CF 3-thiazole-5-base Viscous oil 90-91
*: E-type or Z-type
The geometrical isomer of #13:IV-107
Table 19
No. Q R E B A m.p.(℃)
V-1 V-2 V-3 V-4 V-5 V-6 V-7 V-8 V-9 V-10 V-11 V-12 V-13 V-14 V-15 V-16 V-17 V-18 V-19 V-20 V-21 V-22 V-23 Q9 Q9 Q9 Q9 Q9 Q9 Q9 Q9 Q9 Q9 Q9 Q9 Q9 Q10 Q1O Q1O Q10 Q11 Q11 Q12 Q12 Q12 2-naphthyl 1-Ph 1-Ph 5-Me-1- iPr 5-Me-1- iBu 5-Me-1- sBu 5-Me-1- iBu 5-Me-1- sBu 1-t-Bu 1-t-Bu 1-t-Bu 1-pyridine-2-base 1-pyridine-2-base 1-pyridine-2-base 1-Ph 1-Ph 1-t-Bu 1-t-Bu 1-Me-3-tBu 1-Me-3- tBu Ph Ph Ph - CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN H H H B7 B7 H H B7 H H H B15 B7 B7 H B7 H H B7 H B7 SO 2(4- tBu-Ph) B1 A1 A2 A2 A2 A2 A2 A2 A2 2，6-F 2-Ph A2 A2 A2 A2 A2 A2 A2 A2 A2 A2 A2 A2 A2 A1 148.7-151.3 156-157 78-80 84-89 *99-105 113-114 75-80 vitreousness *111-113 127-129 156.4-158.1 vitreousness *Vitreousness *130-131 207-208 viscous oil viscous oil vitreousness 119-124 247-253 147.5-148.5*174-176.5 viscous oil
Table 19
No. Q R E B A m.p.(℃)
V-24 V-25 V-26 V-27 V-28 V-29 V-30 V-31 V-32 V-33 V-34 V-35 V-36 V-37 V-38 V-39 V-40 V-41 V-42 V-43 V-44 V-45 V-46 2-naphthyl 2-naphthyl Q13 Q1 Q1 Q2 Q2 Q3 Q4 Q4 Q5 Q6 Q7 Q7 Q7 Q8 Q14 Q14 Q14 Q14 Q14 Q14 Q14 - - - 5-Cl 5-Cl 4-Ph 4-t-Bu 3-Ph Ph Ph t-Bu t-Bu 5-CF 3 5-CF 3 5-PhCH 2O 4，6-(MeO) 2 t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu t-Bu CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN H B7 H H B7 H H H H B1 H H H H H H H B7 H B7 B33 H B7 A1 A1 A2 A2 A2 A1 A1 A1 A1 A1 A2 A2 A1 A2 A1 A1 A1 A1 A2 A2 A2 2，6-F 2-Ph 2，6-F 2-Ph 140.1-141.1 viscous oil 121-122 60 decomposes 79.5-81 231-232 218-219 243-245 255.8-256.8 187-190 158-160 215-216 184-185 211-212 220-221 149-155 137.9-143.7 vitreousness 127.5-128.9 vitreousness vitreousness 105.6-108.1 viscous oil: oil
Table 19
No. Q R E B A m.p.(℃)
V-47 V-48 V-49 V-50 V-51 V-52 V-53 V-54 V-55 V-56 V-57 V-58 V-59 V-60 V-61 V-62 V-63 V-64 V-65 V-66 V-67 V-68 V-69 Q14 Q14 Q14 Q14 Q14 Q14 Q14 Q14 Q14 Q14 Q14 Q14 Q14 Q14 Q14 Q14 Q14 Q14 Q14 Q14 Q14 Q14 Q14 Ph Ph Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2，6-F 2-Ph 2，6-F 2-Ph 2，6-F 2-Ph PhCH 2 PhCH 2 PhCH 2 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph 2-Cl-Ph PhMe 2C PhMe 2C CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN H B7 B15 H B7 H B15 B7 H B15 B7 H B15 B7 H CO 2-2-Oct B44 H B45 H SO 2(3-Cl-Ph) H B7 A2 A2 A2 A1 A1 A2 A2 A2 A2 A2 A2 A2 A2 A2 2-MeO-Ph 2-MeO-Ph 2-MeO-Ph 2，6-F 2-Ph 2，6-F 2-Ph A7 A7 A2 A2 113.0-114.9 vitreousness vitreousness 125.5-127.5 104.0-107.5 142.4-143.6 vitreousness vitreousness 136.3-164.7 vitreousness vitreousness 113.2-114.3 vitreousness vitreousness 131.4-132.8 viscous oil vitreousness 155.1-157.9 159.3-160.3 150-152 132-133 vitreousness vitreousness
Table 19
No. Q R E B A m.p.(℃)
V-70 V-71 V-72 V-73 V-74 V-75 V-76 V-77 V-78 V-79 V-80 V-81 V-82 V-83 V-84 V-85 V-86 Q14 Q15 Q16 Q17 Q18 Q19 Q19 Q18 Q18 Q18 Q20 Q20 4-Ph-oxazole-2-base 4-Ph-oxazole-2-base 4-Ph-oxazole-2-base Q19 3-(2-Cl-Ph)-imidazoline-2-ketone-1-base PhMe 2C Ph 3-CN-Ph 5-CO 2Et 3-pyridine-2-base 5-Me-2-Ph 5-Me-2-Ph 3-pyridine-2-base 3-pyridine-2-base t-Bu 6-I 6-I---5-Me-2-Ph- CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN CN COCH 2OMe H H B7 H H B7 B7 B46 H H B7 H B15 B7 H H A2 A1 A1 A2 A2 A2 A2 A2 A2 A2 A2 A2 A2 A2 A2 A7 A2 Vitreousness 151-153 174-175 viscous oil 219 decomposes 181-182 viscous oil vitreousness vitreousness 110.4-110.8 205-208 137-142 165.9-166.7 vitreousness vitreousness 117-118 155-156
*: E-type or Z-type
[example of formulations]
Hereinafter is the pesticide preparation embodiment that contains as the The compounds of this invention of activeconstituents, and still, scope of the present invention is not limited thereto.In following example of formulations, " part " is by weight.
[example of formulations 1] water absorbability pulvis:
50 parts of The compounds of this invention I-1
Zeeklite PFP (trade(brand)name, Zeeklite Mining Industries, 43 parts of Co., the kaolin type clay that Ltd. produces)
Solpol 5050 (Ltd. gives birth to the anion surfactant of 2 parts of products for trade(brand)name, Toho Chemical Co.)
Runox 1000C (Ltd. gives birth to the anion surfactant of 3 parts of products for trade(brand)name, Toho Chemical Co.)
Carplex#80 (Shioogi Pharmaceutical Co., 2 parts of anti-hard caking agents that Ltd. produces)
With mentioned component uniform mixing and grinding, form the water absorbability pulvis.
[example of formulations 2] emulsion:
3 parts of The compounds of this invention I-1
76 parts of methylnaphthalenes
15 parts of isophorones
Solpol 3005X (trade(brand)name, Toho Chemical Co., the nonionogenic tenside of the living 6 parts of products of Ltd. and the mixture of anion surfactant)
Mentioned component is uniformly mixed to form emulsion.
[example of formulations 3] flowing agent:
35 parts of The compounds of this invention I-1
Agrisol S-711 (trade(brand)name, 8 parts of tensio-active agents of nonionic that Kao Corp. produces)
Runox 1000C (Ltd. gives birth to the anion surfactant of 3 parts of products for trade(brand)name, Toho Chemical Co.)
The 1%Rhodopol aqueous solution (trade(brand)name, Rhone-Poulenc gives birth to the thickening material of 20 parts of products)
8 parts of ethylene glycol (antithrombotics)
28.5 parts in water
Mentioned component is uniformly mixed to form flowing agent.
[example of formulations 4] granular water absorbability pulvis (dried flowing agent):
75 parts of The compounds of this invention I-1
Isoban No.1 (trade(brand)name, 10 parts of Co. of Kuraray Isoprene Chemical, the anion surfactant that Ltd. produces)
Vanilex N (trade(brand)name, Sanyo Kokusaku Pulp Co., 5 parts of Ltd.)
Carplex#80 (trade(brand)name, 10 parts of Co. of Shionogi Pharmacetical, the white carbon that Ltd. produces)
With mentioned component uniform mixing and porphyrize, form dried flowing agent.
[example of formulations 5] granula:
0.1 part of The compounds of this invention I-1
55.0 parts of wilkinites
44.9 parts in talcum
With mentioned component uniform mixing and grinding, and, stir, mix and kneading to wherein adding less water.Use extrusion granulator is with gained mixture granulating and be dried to particle.
[example of formulations 6] pulvis:
3.0 parts of The compounds of this invention I-1
Carplex#80 (trade(brand)name, 0.5 part of Co. of Shionogi Pharmacetical, the white carbon that Ltd. produces)
95 parts of clays
1.5 parts of diisopropyl phosphates
With mentioned component uniform mixing and grinding, form pulvis.
During use, water moves 50 to 20000 times of dilution agents with water absorbability pulvis, emulsion, flowing agent and master stream, and uses with the amount of activeconstituents 0.005 to 50kg/ha.
Hereinafter is that the The compounds of this invention hydrobiont adheres to the example of formulations that prevents agent, and still, scope of the present invention is not limited thereto.
[example of formulations 7]
8 parts of The compounds of this invention II-2
7 parts of VYHH (UCC Co., the ethylene type synthetic resins that Ltd. produces)
7 parts of rosin
3 parts of Tritolyl Phosphates
20 parts in talcum
15 parts in barium sulfate
10 parts of red iron oxides
20 parts of dimethylbenzene
10 parts of methyl iso-butyl ketone (MIBK)
Mentioned component is uniformly mixed to form hydrobiont of the present invention to be adhered to and prevents agent.This prevents that agent can be used as coating material.
[example of formulations 8]
5 parts of The compounds of this invention II-2
13 parts of CR-10 (the chlorine rubber resin that Asahi Denka Co., Ltd. produces)
20 parts of the flowers of zinc
20 parts in talcum
2 parts in softening agent
10 parts of red iron oxides
30 parts of dimethylbenzene
Mentioned component is uniformly mixed to form hydrobiont of the present invention to be adhered to and prevents agent.This prevents that agent can be used as coating material.
[example of formulations 9]
8 parts of The compounds of this invention II-2
7 parts of VYHH (UCC Co., the ethylene type synthetic resins that Ltd. produces)
7 parts of rosin
3 parts of Tritolyl Phosphates
20 parts in talcum
15 parts in barium sulfate
10 parts of red iron oxides
20 parts of dimethylbenzene
10 parts of methyl iso-butyl ketone (MIBK)
Mentioned component is uniformly mixed to form hydrobiont of the present invention to be adhered to and prevents agent.This prevents that agent can be used as coating material.
[example of formulations 10]
5 parts of The compounds of this invention II-2
13 parts of CR-10 (the chlorine rubber resin that Asahi Denka KK produces)
20 parts of the flowers of zinc
20 parts in talcum
2 parts in softening agent
10 parts of red iron oxides
30 parts of dimethylbenzene
Mentioned component is uniformly mixed to form hydrobiont of the present invention to be adhered to and prevents agent.This prevents that agent can be used as coating material.
[experimental example]
Following experimental example is in order to the availability of proof The compounds of this invention as pesticides.
Experimental example 1: to Nilaparvata lugen (brown planthopper) ( Nilaparvata lugens Stal) kill the insect test:
5% emulsion (or 25% water absorbability pulvis) of The compounds of this invention is diluted with the water that contains spreading agent, obtain the 500ppm solution of this compound.
Resulting solution fully is applied to plantation on the stem and leaf of the paddy rice in 1/20,000 are of basin.After the chemical solution of being used is done, on each basin, cover columnar coverture in air.In each basin, discharge 10 Nilaparvata lugen (brown planthopper)s ( Nilaparvata lugens) two age nymph.After covering coverture, basin is stored in the thermostatic chamber.After 6 days, observe the insect in each basin, measure insect mortality according to following equation.Each compound divides two groups of basins to test in this way.
Mortality ratio (%)
=[dead insects number/(dead insects number+existence insect number)] * 100
In above-mentioned test, the mortality ratio that following compound exhibits goes out is 80% or higher.
The compounds of this invention: I-2, I-18, I-19, I-23, I-30, I-31, I-32, I-35, I-39, I-42, I-44, I-58, I-59, I-62, I-63, I-70, I-72, I-80, I-106, I-114, I-123, I-137, II-1, II-2, II-3, II-5, II-6, II-12, II-15, II-23, II-25, II-26, II-28, II-33, II-34, II-36, II-37, II-38, II-39, II-43, II-44, II-46, II-53, II-54, II-55, II-61, II-66, II-73, II-74, II-75, II-76, II-80, II-83, II-84, II-85, II-86, II-87, II-88, II-89, II-91, II-92, II-93, II-97, II-98, II-111, II-114, II-116, II-134, II-136, II-137, II-154, II-155, II-159, III-1, III-2, III-4, III-6, III-15, III-16, III-17, III-18, III-19, III-21, IV-48, IV-58, V-2, V-12, V-13, V-28, V-48, V-49, V-51, V-53, V-54, V-55, V-56, V-57, V-59, V-60
Experimental example 2: to rice green leafhopper ( Nephotettix cincticeps Uhler) kill the insect test:
In the The compounds of this invention emulsion that stem and the leaf of crop is immersed in 500ppm about 10 seconds.Stem and the leaf handled are like this put into glass cylinder, will to the organic phosphine insecticide have tolerance rice green leafhopper ( Nephotettix cincticeps) adult puts into wherein.Each glass cylinder is covered the coverture of punching, and be stored in 25 ℃ the thermostatic chamber.After 6 days, observe the insect in each cylinder, and according to experimental example 1 in identical equation measure mortality ratio.Each compound is divided into two groups of cylinders in this way to be tested.In above-mentioned test, the mortality ratio that following compound exhibits goes out is 80% or higher.
The compounds of this invention: I-1, I-2, I-4, I-5, I-8, I-9, I-10, I-19, I-24, I-29, I-30, I-31, I-32, I-33, I-34, I-35, I-36, I-39, I-40, I-41, I-42, I-43, I-44, I-47, I-53, I-54, I-55, I-56, I-57, I-58, I-59, I-62, I-63, I-69, I-70, I-71, I-72, I-74, I-79, I-80, I-81, I-115, I-121, I-125, I-127, I-137, II-1, II-2, II-3, II-5, II-6, II-7, II-9, II-10, II-11, II-12, II-13, II-15, II-23, II-26, II-28, II-33, II-34, II-36, II-38, II-37, II-43, II-46, II-49, II-52, II-54, II-55, II-63, II-64, II-65, II-66, II-67, II-68, II-69, II-73, II-74, II-75, II-76, II-77, II-78, II-79, II-80, II-81, II-83, II-84, II-85, II-86, II-87, II-88, II-89, II-91, II-92, II-93, II-97, II-98, II-99, II-107, II-111, II-116, II-117, II-130, II-131, II-132, II-134, II-136, II-137, II-142, II-145, II-153, II-154, III-1, III-2, III-3, III-4, III-5, III-6, III-13, III-15, III-16, III-17, III-18, III-19, III-20, III-21, IV-32, IV-58, V-2, V-12, V-13, V-14, V-38, V-41, V-43, V-48, V-49, V-51, V-53, V-54, V-55, V-56, V-57, V-59, V-60, V-75
Experimental example 3: to black peach aphid ( Myzus persicae Sulzer) insect test extremely:
Wet filter paper is put into the laboratory glass disc of each internal diameter 3cm, and the cabbage leaves identical with the diameter of dish is placed on the filter paper.With 4 female black peach aphids ( Myzus persicae) no wing adult is placed on the cabbage leaves.Second day, use the rotation sprinkler, with compound sample (2.5mg/cm 2) be sprayed on the dish.Compound solution described herein is by 5% emulsion (or 25% water absorbability pulvis) of The compounds of this invention is diluted to 500ppm makes with containing the water of spreading agent.After 6 days, observe the insect in each dish, measure insect (larva and adult) mortality ratio according to following equation.Each compound divides two groups of dishes to test in this way.
Mortality ratio (%)
=[dead insects number/(dead insects number+existence insect number)] * 100
In above-mentioned test, the mortality ratio that following compound exhibits goes out is 80% or higher.
The compounds of this invention: I-1, I-2, I-3, I-4, I-5, I-7, I-8, I-9, I-10, I-11, I-12, I-13, I-14, I-16, I-17, I-18, I-19, I-21, I-22, I-23, I-24, I-25, I-26, I-27, I-28, I-29, I-30, I-31 I-32, I-33, I-34, I-35, I-36, I-37, I-38, I-40, I-41, I-42, I-43, I-44, I-45, I-46, I-47, I-48, I-51, I-52, I-53, I-54, I-55, I-56, I-57, I-58, I-59, I-62, I-63, I-69, I-70, I-71, I-72, I-73, I-74, I-76, I-77, I-78, I-79, I-80, I-81, I-84, I-85, I-86, I-89, I-90, I-92, I-96, I-97, I-104, I-108, I-125, I-136, I-137, I-138, II-2, II-3, II-5, II-6, II-7, II-8, II-9, II-10, II-11, II-12, II-15, II-16, II-17, II-23, II-24, II-25, II-26, II-27, II-28, II-33, II-34, II-35, II-36, II-37, II-38, II-39, II-43, II-44, II-50, II-52, II-53, II-54, II-55, II-58, II-60, II-63, II-64, II-65, II-66, II-68, II-69, II-70, II-71, II-73, II-74, II-75, II-76, II-78, II-79, II-83, II-84, II-85, II-86, II-87, II-88, II-89, II-90, II-91, II-92, II-93, II-97, II-98, II-99, II-101, II-102, II-105, II-107, II-111, II-116, II-117, II-118, II-121, II-130, II-131, II-132, II-133, II-134, II-136, II-137, II-138, II-140, II-141, II-142, II-151, II-153, II-154, II-159, II-160, III-1, III-2, III-3, III-4, III-5, III-6, III-15, III-16, III-17, III-18, III-19, III-20, III-21, IV-10, IV-11, IV-21, IV-23, IV-45, V-1, V-2, V-10, V-11, V-12, V-13, V-14, V-28, V-31, V-32, V-41, V-45, V-48, V-49, V-50, V-51, V-52, V-53, V-54, V-55, V-56, V-57, V-59, V-60, V-73, V-75
Experimental example 4: to small cabbage moth ( Plutella xylosttella Linne) kill the insect test:
Cabbage leaves was immersed in the The compounds of this invention water miscible liquid of 500ppm about 10 seconds.After in air, doing, the leaf of handling is like this put into test board.Each the dish in discharge 10 small cabbage moths ( Plutella xylosttella Linne) larva (second larvae).With foraminous coverture on each disk cover, and be stored in 25 ℃ the thermostatic chamber.After 6 days, observe the insect in each dish, and according to experimental example 1 in identical equation measure insect mortality.Each compound is divided into two groups of plates in this way to be tested.In above-mentioned test, the mortality ratio that following compound exhibits goes out is 80% or higher.
The compounds of this invention: I-1, I-2, I-4 I-5, I-6, I-8, I-9, I-10, I-13, I-18, I-19, I-29, I-30, I-31, I-33, I-34, I-35, I-36, I-38, I-39, I-40, I-41, I-43, I-44, I-45, I-46, I-47, I-51, I-52, I-53, I-56, I-57, I-58, I-59, I-62, I-63, I-70, I-71, I-72, I-73, I-74, I-76, I-77, I-78, I-79, I-80, I-81, I-84, I-86, I-89, I-96, I-97, I-99, I-104, I-106, I-114, I-125, I-137, II-1, II-2, II-5, II-6, II-7, II-8, II-9, II-10, II-11, II-12, II-13, II-15, II-17, II-23, II-24, II-25, II-26, II-27, II-28, II-33, II-34, II-35, II-36, II-37, II-38, II-39, II-40, II-41, II-42, II-43, II-54, II-55, II-58, II-60, II-61, II-62, II-63, II-64, II-65, II-66, II-67, II-68, II-69, II-70, II-71, II-72, II-73, II-74, II-75, II-76, II-77, II-78, II-79, II-80, II-81, II-83, II-84, II-85, II-86, II-87, II-88, II-89, II-90, II-91, II-92, II-93, II-94, II-97, II-98, II-99, II-100, II-101, II-105, II-106, II-107, II-108, II-109, II-110, II-111, II-116, II-117, II-118, II-121, II-122, II-155, II-159, II-161, III-1, III-2, III-3, III-4, III-5, III-6, III-7, III-9, III-10, III-11, III-13, III-14, III-15, III-16, III-17, III-18, III-19, III-20, III-21, IV-7, IV-8, IV-29, IV-47, IV-53, IV-58, V-1, V-2, V-11, V-12, V-13, V-29, V-37, V-41, V-43, V-46, V-48, V-50, V-51, V-52, V-53, V-54, V-55, V-56, V-57, V-58, V-59, V-60, V-64, V-75
Experimental example 5: to aulacophora femoralis ( Aulacophora femoralisMotschuulsky) the insect that kills is tested:
With 5% emulsion (or the 25% water absorbability pulvis) dilution of the water that contains spreading agent, obtain the 500ppm solution of this compound with The compounds of this invention.Folium Cucumidis sativi was immersed in the above-mentioned chemical solution about 10 seconds,, puts into experiment plate again at air drying.With 10 aulacophora femoralises ( Aulacophora femoralis) two age nymph put into each the dish.With coverture on each disk cover, and be stored in the thermostatic chamber.After 6 days, observe the insect in each dish, and according to experimental example 1 in identical equation measure insect mortality.Each compound is divided into two groups of dishes in this way to be tested.In above-mentioned test, the mortality ratio that following compound exhibits goes out is 80% or higher.
The compounds of this invention: I-1, I-2, I-4, I-6, I-8, I-9, I-10, I-11, I-12, I-13, I-29, I-30, I-31, I-32, I-33, I-34, I-35, I-39, I-40, I-41, I-43, I-44, I-46, I-53, I-54, I-55, I-56, I-57, I-58, I-59, I-61, I-62, I-63, I-69, I-70, I-71, I-72, I-74, I-76, I-77, I-78, I-79, I-80, I-81, I-82, I-83, I-92, I-101, I-103, I-104, I-108, I-109, I-124, I-127, I-128, II-1, II-6, II-7, II-8, II-9, II-10, II-11, II-12, II-13, II-14, II-15, II-16, II-17, II-23, II-24, II-25, II-26, II-27, II-28, II-33, II-34, II-35, II-36, II-37, II-38, II-39, II-41, II-42, II-43, II-47, II-50, II-53, II-54, II-55, II-57, II-58, II-61, II-62, II-63, II-65, II-66, II-99, II-101, II-102, II-104, II-105, II-106, II-107, II-108, II-109, II-110, II-114, II-122, II-124, II-125, II-131, II-132, II-133, II-134, II-136, II-137, II-139, II-140, II-141, II-142, II-153, II-154, III-1, III-2, III-3, III-4, III-5, III-6, III-9, III-10, III-11, III-12, III-14, III-15, III-16, III-17, III-20, IV-6, IV-13, IV-33, IV-39, IV-56, IV-60, IV-61, IV-72, IV-82, V-1, V-2, V-11, V-12, V-13, V-17, V-22, V-26, V-27, V-29, V-37, V-40, V-42, V-48, V-49, V-50, V-51, V-52, V-54, V-55, V-57, V-59, V-60, V-61, V-64, V-75
EXPERIMENTAL EXAMPLE 6: to T.urticae Koch ( Tetranychus urticae Koch) kill the mite test:
With the shot hole of leaf device Kidney bean shot hole of leaf is obtained the disk of 3cm diameter, and put it on the wet filter paper in 7cm diameter vinylbenzene cup.Every leaf put 10 T.urticae Koches ( Tetranychus Urticae) larva.With 5% emulsion (or 25% water absorbability pulvis) of the water dilution The compounds of this invention that contains spreading agent, obtain the 500ppm solution of this compound.Use the rotation sprinkler, solution is sprayed into each cup, and cup is stored in 25 ℃ the thermostatic chamber with the amount of 2ml/ cup.After 96 hours, observe the mite in each glass, and according to experimental example 1 in identical equation measure the mortality ratio of mite.Each compound is divided into two groups of cups in this way to be tested.In above-mentioned test, the mortality ratio that following compound exhibits goes out is 80% or higher.
The compounds of this invention: I-1, I-2, I-3, I-4, I-5, I-7, I-8, I-9, I-10, I-12, I-13, I-19, I-24, I-25, I-26, I-27, I-28, I-29, I-30, I-31, I-32, I-33, I-34, I-35, I-36, I-38, I-40, I-41, I-42, I-43, I-44, I-45, I-46, I-47, I-48, I-50, I-51, I-52, I-55, I-56, I-57, I-58, I-59, I-60, I-61, I-62, I-63, I-70, I-71, I-72, I-74, I-76, I-80, I-94, I-95, I-96, I-97, I-99, I-101, I-102, I-103, I-104, I-105, I-106, I-108, I-109, I-110, I-111, I-112, I-113, I-114, I-115, I-117, I-118, I-119, I-122, I-123, I-124, I-125, I-126, I-127, I-128, I-137, II-2, II-3, II-5, II-6, II-7, II-8, II-9, II-10, II-11, II-12, II-13, II-15, II-16, II-17, II-23, II-25, II-26, II-27, II-28, II-33, II-34, II-35, II-36, II-37, II-38, II-39, II-40, II-41, II-42, II-43, II-45, II-46, II-47, II-48, II-50, II-52, II-53, II-54, II-55, II-58, II-59, II-60, II-61, II-63, II-64, II-65, II-66, II-67, II-68, II-69, II-70, II-71, II-72, II-73, II-74, II-75, II-76, II-77, II-78, II-79, II-80, II-81, II-83, II-84, II-85, II-86, II-87, II-88, II-89, II-90, II-91, II-92, II-93, II-95, II-97, II-98, II-99, II-101, II-102, II-103, II-105, II-106, II-107, II-108, II-109, II-110, II-111, II-116, II-117, II-118, II-133, II-134, II-136, II-137, II-151, II-153, II-154, II-155, II-159, II-160, II-161, II-173, III-3, III-4, III-5, III-6, III-7, III-9, III-10, III-11, III-12, III-15, III-17, III-18, III-19, III-21, IV-1, IV-2, IV-3, IV-4, IV-5, IV-7, IV-10, IV-11, IV-12, IV-13, IV-14, IV-16, IV-17, IV-18, IV-19, IV-20, IV-21, IV-22, IV-24, IV-25, IV-26, IV-28, IV-29, IV-33, IV-35, IV-36, IV-39, IV-40, IV-41, IV-42, IV-43, IV-44, IV-45, IV-46, IV-47, IV-48, IV-49, IV-50, IV-51, IV-54, IV-55, IV-56, IV-58, IV-59, IV-60, IV-61, IV-62, IV-63, IV-64, IV-65, IV-66, IV-67, IV-68, IV-69, IV-70, IV-71, IV-72, IV-74, IV-75, IV-76, IV-79, IV-80, IV-82, IV-94, IV-95, IV-96, IV-99, IV-100, IV-101, IV-102, IV-109, IV-110, IV-111, IV-112, V-1, V-2, V-3, V-4, V-5, V-6, V-7, V-8, V-10, V-11, V-12, V-13, V-14, V-15, V-16, V-17, V-19, V-23, V-24, V-25, V-26, V-28, V-31, V-36, V-37, V-38, V-40, V-41, V-42, V-43, V-44, V-46, V-47, V-48, V-49, V-50, V-51, V-52, V-53, V-54, V-55, V-56, V-57, V-58, V-59, V-60, V-73, V-75
Experimental example 7: the prevention wheat leaf rust ( Puccinia reconditaEx Desmazi é re) test
Water is diluted to 500ppm with the The compounds of this invention emulsion and obtains compound solution, uses atomizer, with the amount of 20ml/ basin this solution is sprayed on the wheat (Norin No.61) of long to 1.5 to 2.0 leaf phases in the 5.5cm diameter basin.
Second day, with wheat leaf rust infective pathogen body ( Puccinia recondita) spore suspension (2 * 10 5Spore/ml) be sprayed in the crop basin, and be that 25 ℃, humidity are 95% or are higher than to place in 95% the inoculation tank and spend the night with basin in temperature.Then, basin is placed in the greenhouse.Inoculate after 7 days, measure area ratio formed infection and that spore is arranged on the inoculation leaf, and according to following Equation for Calculating prevention value.
The prevention value
=[1-(infection and the spotted area ratio in infection in the treatment zone and the spotted area ratio/district of being untreated)] * 100
In above-mentioned test, the prevention value of following compound is 70 to 100.
The compounds of this invention: I-9, I-108, I-127, I-128, II-14, II-15, IV-2, IV-7, V-15, V-10.
Industrial applicibility
Because life-time service sterilant and microbicide, some insects become pharmaceutical chemicals are had tolerance, and are difficult to usually eliminate with common insecticides and microbicide.In addition, some sterilant toxicity are big, and are easy to residually for a long time, and do not decompose, and destroy thereby the ecosystem produced.Therefore, the invention provides sterilant and the mycocide short new, low toxicity, and provide the ecosystem almost do not had influence and cause the hydrobiont of secondary pollution to adhere to hardly and prevent agent with long-lasting.

Claims (7)

1, formula (I) ethene derivatives:
Wherein:
The thiazolyl that the Q representative is replaced by R arbitrarily;
The heterocyclic radical that the A representative is replaced by Y arbitrarily, described heterocyclic radical is a thienyl, furyl, pyrryl oxazolyl isoxazolyl, thiazolyl, isothiazolyl, pyrazolyl, imidazolyl, 1,3,4-oxadiazole base, 1,2,4-oxadiazole base, 1,3, the 4-thiadiazolyl group, 1,2, the 4-thiadiazolyl group, 1,2, the 4-triazolyl, 1,2, the 3-thiadiazolyl group, 1,2, the 3-triazolyl, 1,2,3, the 4-tetrazyl, pyridyl, pyrimidyl, pyrazinyl, pyridazinyl, 1,3, the 5-triazinyl, 1,2, the 4-triazinyl, pyrazolinyl, imidazolinyl oxazolinyl isoxazoline-3-yl, thiazolinyl, 3 (2H)-pyridazinones, benzothiazolyl, benzimidazolyl-, indazolyl benzoxazolyl, quinolyl, isoquinolyl, quinoxalinyl, 2, the 3-phthalazinyl, cinnoline base or quinazolyl;
B represents H, C 1-C 4Alkyl, C 1-C 4Haloalkyl, C 2-C 4Alkoxyalkyl, CH 3SCH 2, CH 3OC 2H 4OCH 2, the C that is replaced by phenyl 1-C 4Alkyl, and described phenyl is arbitrarily by halogen or C 1-C 4Alkyl replaces, the C that is replaced by benzoyl 1-C 4Alkyl, and described benzoyl is arbitrarily by halogen or C 1-C 4Alkyl replaces, THP trtrahydropyranyl, (CH 3) 3Si, C 1-C 4Alkyl sulphonyl is arbitrarily by halogen or C 1-C 4The benzenesulfonyl that alkyl replaces ,-SO 2CF 3, C 1-C 4The alkyl monosubstituted amino alkylsulfonyl, C 2-C 8Dialkyl amino sulfonyl, phenyl amino alkylsulfonyl, C 2-C 5The alkyl monosubstituted amino thiocarbonyl, C 3-C 9The dialkyl amido thiocarbonyl, C 2-C 5The cyano group alkyl, C 3-C 9Alkoxy carbonyl alkyl ,-C (=O) T 1,-P (=O) T 2T 3,-P (=S) T 2T 3, alkali metal atom, alkaline earth metal atom, or NHT 4T 5T 6
Condition is: when Q was the 2-thiazolyl, B was C 1-C 4Alkyl, C 1-C 4Haloalkyl, C 2-C 4Alkoxyalkyl, CH 3SCH 2, CH 3OC 2H 4OCH 2, the C that is replaced by phenyl 1-C 4Alkyl, and described phenyl is arbitrarily by halogen or C 1-C 4Alkyl replaces, the C that is replaced by benzoyl 1-C 4Alkyl, and described benzoyl is arbitrarily by halogen or C 1-C 4Alkyl replaces, THP trtrahydropyranyl, (CH 3) 3Si, C 1-C 4Alkyl sulphonyl is arbitrarily by halogen or C 1-C 4The benzenesulfonyl that alkyl replaces ,-SO 2CF 3, C 1-C 4The alkyl monosubstituted amino alkylsulfonyl, C 2-C 8Dialkyl amino sulfonyl, phenyl amino alkylsulfonyl, C 2-C 5The alkyl monosubstituted amino thiocarbonyl, C 3-C 9The dialkyl amido thiocarbonyl, C 2-C 5The cyano group alkyl, C 3-C 9Alkoxy carbonyl alkyl ,-C (=O) T 1,-P (=O) T 2T 3, or-P (=S) T 2T 3
E represents CN;
R is the substituting group that freely is selected from following radicals: halogen atom, C 1-C 10Alkyl, the C that is replaced by phenyl 1-C 4Alkyl, and described phenyl is arbitrarily by halogen or C 1-C 4Alkyl replaces, C 2-C 6Alkenyl, C 2-C 6Alkynyl, C 1-C 6Haloalkyl, C 2-C 6Halogenated alkenyl, C 2-C 6The halo alkynyl, C 3-C 6Halogenated cycloalkyl is arbitrarily by C 1-C 3The C that alkyl replaces 3-C 6Cycloalkyl, C 1-C 6Alkoxyl group, C 2-C 6Alkenyloxy, C 2-C 6Alkynyloxy group, C 1-C 4Halogenated alkoxy, C 2-C 6The halo alkenyloxy, C 2-C 6The halo alkynyloxy group, C 1-C 4Alkylthio, C 1-C 4Alkyl sulphinyl, C 1-C 4Alkyl sulphonyl, C 2-C 6Alkenyl thio, C 2-C 6The alkenyl sulfinyl, C 2-C 6The alkenyl alkylsulfonyl, C 2-C 6The alkynes sulfenyl, C 2-C 6The alkynyl sulfinyl, C 2-C 6The alkynyl alkylsulfonyl, C 1-C 4Halogenated alkylthio, C 1-C 4The haloalkyl sulfinyl, C 1-C 4Halogenated alkyl sulfonyl, C 2-C 6The halo alkenyl thio, C 2-C 6The halogenated alkenyl sulfinyl, C 2-C 6The halogenated alkenyl alkylsulfonyl, C 2-C 6The acetylenic halide sulfenyl, C 2-C 6Halo alkynyl sulfinyl, C 2-C 6Halo alkynyl alkylsulfonyl, NO 2, CN ,-NU 1U 2, phenoxy group, OH, naphthyl, C 2-C 7Carbalkoxy, C 2-C 4Alkoxyalkyl, C 2-C 4Alkyl-carbonyl, C 2-C 5Alkyl carbonyl oxy, C 2-C 5Haloalkyl carbonyl oxygen base, the benzoyl that is replaced by X arbitrarily, the phenyl that is replaced by X arbitrarily, the pyridyl that is replaced by X arbitrarily, arbitrarily the thienyl that is replaced by X and-N=CT 7T 8,
Condition is when substituting group is two or more, and described substituting group can be identical or different,
And the quantity of substituent R is 1 or 2;
Or R is bonded on adjacent the position of substitution to form the alkylidene group of 5,6,7 or 8 yuan of rings;
Y is the substituting group that freely is selected from following radicals: halogen atom, C 1-C 10Alkyl, C 1-C 6Haloalkyl, C 1-C 6Alkoxyl group, C 2-C 6Alkenyloxy, C 2-C 6Alkynyloxy group, C 1-C 4Halogenated alkoxy, C 2-C 6The halo alkenyloxy, C 2-C 6The halo alkynyloxy group, C 1-C 4Alkylthio, C 1-C 4Alkyl sulphinyl, C 1-C 4Alkyl sulphonyl, C 2-C 6Alkenyl thio, C 2-C 6The alkenyl sulfinyl, C 2-C 6The alkenyl alkylsulfonyl, C 2-C 6The alkynes sulfenyl, C 2-C 6The alkynyl sulfinyl, C 2-C 6The alkynyl alkylsulfonyl, C 1-C 4Halogenated alkylthio, C 1-C 4The haloalkyl sulfinyl, C 1-C 4Halogenated alkyl sulfonyl, C 2-C 6The halo alkenyl thio, C 2-C 6The halogenated alkenyl sulfinyl, C 2-C 6The halogenated alkenyl alkylsulfonyl, C 2-C 6The acetylenic halide sulfenyl, C 2-C 6Halo alkynyl sulfinyl, C 2-C 6Halo alkynyl alkylsulfonyl, NO 2, CN ,-NU 1U 2, OH, C 2-C 7Carbalkoxy, C 2-C 4Alkoxyalkyl, C 2-C 5Alkyl carbonyl oxy, C 2-C 5Haloalkyl carbonyl oxygen base, C 3-C 7Dialkyl amido carbonyl oxygen base, arbitrarily the phenyl that is replaced by X and-N=CT 7T 8, T wherein 7And T 8Independent separately H or phenyl, benzyl or the C of representing 1-C 6Alkyl, or T 7And T 8Can form 5,6,7 or 8 yuan of rings with the carbon atom of institute's bonding,
Condition is when substituting group is two or more, and described substituting group can be identical or different,
And the quantity of substituting group Y is 1,2,3 or 4;
Or Y is bonded on adjacent the position of substitution to form the alkylidene group of 5,6,7 or 8 yuan of rings;
T 1Represent C 1-C 20Alkyl, C 2-C 6Alkenyl, C 1-C 6Haloalkyl, C 1-C 4Alkoxy-C 1-C 4Alkyl, C 3-C 6Halogenated cycloalkyl, the C that is replaced by phenyl 1-C 4Alkyl, and described phenyl is arbitrarily by halogen or C 1-C 4Alkyl replaces, arbitrarily by C 1-C 3The C that alkyl replaces 3-C 6Cycloalkyl, the cycloalkyl that is replaced by phenyl, and described phenyl is arbitrarily by halogen or C 1-C 4Alkyl replaces, by phenyl and C 1-C 4The common cyclopropyl that replaces of alkyl, and described phenyl is arbitrarily by halogen or C 1-C 4Alkyl replaces, by phenyl and the common C that replaces of halogen 3-C 4Cycloalkyl, and described phenyl is arbitrarily by halogen or C 1-C 4Alkoxyl group replaces, by C 2-C 4Alkenyl and C 1-C 4The common cyclopropyl that replaces of alkyl, and described C 2-C 4Alkenyl is replaced by halogen arbitrarily, the C that is replaced by phenyl 2-C 4Alkenyl, and described phenyl is arbitrarily by halogen or C 1-C 4Alkyl replaces, C 1-C 12Alkoxyl group, C 1-C 4Halogenated alkoxy, C 2-C 5Alkenyloxy is arbitrarily by C 1-C 3The C that alkyl replaces 3-C 6Cycloalkyloxy, benzyloxy, C 2-C 5Carbalkoxy ,-NU 1U 2, phenyl amino, the phenyl that is replaced by Z arbitrarily, the phenoxy group that is replaced by Z, the thiophenyl that is replaced by Z, the naphthyl that is replaced by Z arbitrarily arbitrarily arbitrarily, or 5 yuan or 6 yuan of heterocyclic radicals being replaced by Z arbitrarily, described heterocyclic radical is selected from thienyl, furyl, pyrryl oxazolyl isoxazolyl, thiazolyl, isothiazolyl, pyrazolyl, imidazolyl, 1,3,4-oxadiazole base, 1,2,4-oxadiazole base, 1,3, the 4-thiadiazolyl group, 1,2, the 4-thiadiazolyl group, 1,2, the 4-triazolyl, 1,2, the 3-thiadiazolyl group, 1,2, the 3-triazolyl, 1,2,3, the 4-tetrazyl, pyridyl, pyrimidyl, pyrazinyl, pyridazinyl, the 1,3,5-triazines base, 1,2, the 4-triazinyl, pyrazolinyl, imidazolinyl oxazolinyl isoxazoline-3-yl, thiazolinyl and 3 (2H)-pyridazinone;
T 2And T 3Independently represent OH, phenyl, C separately 1-C 6Alkyl, C 1-C 6Alkoxyl group or C 1-C 4Alkylthio;
T 4, T 5And T 6The independent separately H, C of representing 1-C 6Alkyl, C 2-C 6Alkenyl is arbitrarily by C 1-C 3The C that alkyl replaces 3-C 6Cycloalkyl, or benzyl; Or T 4, T 5And T 6In any two can form 5,6,7 or 8 yuan of cyclic groups with the nitrogen-atoms of institute's bonding, and described cyclic group contains aerobic, nitrogen and/or sulphur atom arbitrarily;
X and Z freely are selected from halogen atom, C independently 1-C 4Alkyl, C 1-C 4Haloalkyl, C 1-C 4Alkoxyl group, C 1-C 4Halogenated alkoxy, C 1-C 4Alkylthio, C 1-C 4Alkyl sulphinyl, C 1-C 4Alkyl sulphonyl, C 2-C 5Alkenyl thio, C 2-C 5The alkenyl sulfinyl, C 2-C 5The alkenyl alkylsulfonyl, C 1-C 4Halogenated alkylthio, C 1-C 4The haloalkyl sulfinyl, C 1-C 4Halogenated alkyl sulfonyl, NO 2, CN, CHO, OH ,-NU 1U 2, phenyl, phenoxy group, C 2-C 5Carbalkoxy,
Condition is when substituting group is two or more, and described substituting group can be identical or different,
And the quantity of substituent X and Z each naturally 1,2,3,4 or 5;
T 7And T 8Independently represent H separately, or phenyl, benzyl, or C 1-C 6Alkyl; Or T 7And T 8Can form 5,6,7 or 8 yuan of rings with the carbon atom of institute's bonding; And
U 1And U 2The independent separately H, C of representing 1-C 6Alkyl, C 2-C 5Alkyl-carbonyl, phenyl or benzyl; Or U 1And U 2Can form 5,6,7 or 8 yuan of rings with the nitrogen-atoms of institute's bonding.
2, ethene derivatives as claimed in claim 1, wherein:
A is the heterocyclic radical that is replaced by Y arbitrarily, and described heterocyclic radical is thienyl, furyl, pyrryl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, pyrazolyl, imidazolyl, 1,3,4-oxadiazole base, 1,2,4-oxadiazole base, 1,3,4-thiadiazolyl group, 1,2,4-thiadiazolyl group, 1,2,4-triazolyl, 1,2,3-thiadiazolyl group, 1,2,3-triazolyl, 1,2,3,4-tetrazyl, pyridyl, pyrimidyl, pyrazinyl, pyridazinyl, 1,3,5-triazines base, 1,2,4-triazinyl, pyrazolinyl or imidazolinyl;
B is H, C 1-C 4Alkyl, C 1-C 4Haloalkyl, C 2-C 4Alkoxyalkyl, CH 3OC 2H 4OCH 2, C 1-C 4Alkyl sulphonyl is arbitrarily by halogen or C 1-C 4The benzenesulfonyl that alkyl replaces ,-SO 2CF 3, C 2-C 8Dialkyl amino sulfonyl, C 2-C 9The dialkyl amido thiocarbonyl, C 3-C 9Alkoxy carbonyl alkyl ,-C (=O) T 1,-P (=O) T 2T 3,-P (=S) T 2T 3, alkali metal atom, alkaline earth metal atom, or NHT 4T 5T 6
T 1Be C 1-C 20Alkyl, C 2-C 6Alkenyl, C 1-C 4Haloalkyl, C 1-C 4Alkoxy-C 1-C 4Alkyl, the C that is replaced by phenyl 1-C 4Alkyl, and described phenyl is arbitrarily by halogen or C 1-C 4Alkyl replaces, C 3-C 6Halogenated cycloalkyl is arbitrarily by C 1-C 3The C that alkyl replaces 3-C 6Cycloalkyl, the cycloalkyl that is replaced by phenyl, and described phenyl is arbitrarily by halogen or C 1-C 4Alkyl replaces, by phenyl and C 1-C 4The common cyclopropyl that replaces of alkyl, and described phenyl is arbitrarily by halogen or C 1-C 4Alkyl replaces, by phenyl and the common C that replaces of halogen 3-C 4Cycloalkyl, and described phenyl is arbitrarily by halogen or C 1-C 4Alkoxyl group replaces, by C 2-C 4Alkenyl and C 1-C 4The cyclopropyl that alkyl replaces, and described C 2-C 4Alkenyl is replaced by halogen arbitrarily, the C that is replaced by phenyl 2-C 4Alkenyl, and described phenyl is arbitrarily by halogen or C 1-C 4Alkyl replaces, C 1-C 12Alkoxyl group, C 1-C 4Halogenated alkoxy, C 2-C 5Alkenyloxy is arbitrarily by C 1-C 3The C that alkyl replaces 3-C 6Cycloalkyloxy, benzyloxy, C 2-C 5Carbalkoxy, the phenyl that is replaced by Z arbitrarily, the phenoxy group that is replaced by Z arbitrarily, thiophenyl, naphthyl, or the heterocyclic radical that is replaced by Z arbitrarily, described heterocyclic radical are selected from thienyl, furyl, oxazolyl, thiazolyl, pyrazolyl and pyridyl.
3, ethene derivatives as claimed in claim 2, wherein:
Q is the thiazolyl that is replaced by R arbitrarily, for
Or
A is the heterocyclic radical that is replaced by Y arbitrarily, and described heterocyclic radical is
Or
Condition is:
Y 1Be selected from: halogen atom, C 1-C 10Alkyl, C 1-C 6Haloalkyl, C 1-C 6Alkoxyl group, C 2-C 6Alkenyloxy, NO 2, CN ,-NU 1U 2, OH, C 2-C 7Carbalkoxy, C 2-C 4Alkoxyalkyl, arbitrarily the phenyl that is replaced by X and-N=CT 7T 8, T wherein 7And T 8Independent separately H or phenyl, benzyl or the C of representing 1-C 6Alkyl, or T 7And T 8Can form 5,6,7 or 8 yuan of rings with the carbon atom of institute's bonding, or can with adjacent Y 1Form 5,6,7 or 8 yuan of rings as alkylidene group together;
X is that quantity is 1 to 4 and freely is selected from the substituting group of following group: halogen atom, C 1-C 4Alkyl, C 1-C 4Haloalkyl, C 1-C 4Alkoxyl group, C 1-C 4Halogenated alkoxy, C 1-C 4Alkylthio, C 1-C 4Alkyl sulphinyl, C 1-C 4Alkyl sulphonyl, C 2-C 5Alkenyl thio, C 2-C 5The alkenyl sulfinyl, C 2-C 5The alkenyl alkylsulfonyl, C 1-C 4Halogenated alkylthio, C 1-C 4The haloalkyl sulfinyl, C 1-C 4Halogenated alkyl sulfonyl, NO 2, CN, CHO, OH ,-NU 1U 2, phenyl, phenoxy group, and C 2-C 5Carbalkoxy,
Condition is when the quantity of substituent X is two or more, and described substituting group can be identical or different;
Z is that quantity is 1 to 4 and freely is selected from the substituting group of following group: halogen atom, C 1-C 4Alkyl, C 1-C 4Haloalkyl, C 1-C 4Alkoxyl group, C 1-C 4Halogenated alkoxy, C 1-C 4Alkylthio, C 1-C 4Alkyl sulphinyl, C 1-C 4Alkyl sulphonyl, C 1-C 4Alkenyl thio, C 1-C 4The alkenyl sulfinyl, C 1-C 4The alkenyl alkylsulfonyl, NO 2, CN ,-NU 1U 2, phenyl, phenoxy group, and C 2-C 5Carbalkoxy,
Condition is when the quantity of substituting group Z is two or more, and described substituting group can
With identical or different;
M represents substituent quantity, and is 0,1,2 or 3;
N represents substituent quantity, and is 0,1,2,3 or 4;
P represents substituent quantity, and is 0,1 or 2;
Q represents substituent quantity, and is 0 or 1;
Condition is when each integer 2 or when bigger, described substituting group can be identical or different naturally of m, n and p,
Other substituting groups and symbol definition are with claim 1.
4, ethene derivatives as claimed in claim 2, wherein A is the thiazolyl that is replaced by Y arbitrarily, the pyrazolyl that is replaced by Y arbitrarily, the pyridyl that is replaced by Y, or the pyrimidyl that is replaced by Y arbitrarily arbitrarily.
5, ethene derivatives as claimed in claim 3, wherein:
Q is
Figure C971940410010C1
Or
A is
Figure C971940410011C1
Figure C971940410011C2
Or
Y 1Be halogen atom, C 1-C 4Alkyl, C 1-C 4Haloalkyl, C 1-C 4Alkoxyl group, NO 2, CN, or C 2-C 5Carbalkoxy; And
Y 2Be halogen atom, C 1-C 4Alkyl, C 1-C 6Haloalkyl, C 2-C 4Alkoxyalkyl, or the phenyl that is replaced by X arbitrarily,
Other substituting groups and symbol definition are with claim 1.
6, ethene derivatives as claimed in claim 1, described derivative is selected from:
Figure C971940410011C4
Figure C971940410012C1
Figure C971940410012C2
Or
7, agricultural chemicals, described agricultural chemicals contain as the described ethene derivatives of one or more claims 1 to 6 of activeconstituents, are insecticide, miticide or mycocide.
CNB97194041XA 1996-04-25 1997-04-24 Ethylene derivatives and pest controlling agents Expired - Lifetime CN1227229C (en)

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EP0913392A4 (en) 1999-12-15
CA2252536A1 (en) 1997-10-30
TW449460B (en) 2001-08-11
DE69723267D1 (en) 2003-08-07
US6063734A (en) 2000-05-16
EP0913392B1 (en) 2003-07-02
US20070049495A1 (en) 2007-03-01
US6462049B1 (en) 2002-10-08
IL126728A0 (en) 1999-08-17
ES2201293T3 (en) 2004-03-16
US20030216394A1 (en) 2003-11-20
USRE38188E1 (en) 2003-07-15
US7037880B2 (en) 2006-05-02
CN1216530A (en) 1999-05-12
CA2252536C (en) 2010-04-06
CN101817784A (en) 2010-09-01
AU736854B2 (en) 2001-08-02
PT913392E (en) 2003-11-28
EP1360901A1 (en) 2003-11-12
IL126728A (en) 2009-12-24
BR9709126A (en) 2000-01-11
WO1997040009A1 (en) 1997-10-30
AU2407197A (en) 1997-11-12
EP0913392A1 (en) 1999-05-06
CN101817784B (en) 2012-02-01
DE69723267T2 (en) 2004-04-22
ATE244219T1 (en) 2003-07-15

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